Canonical Allele Identifier: CA1148224343
Gene: MUTYH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45331219_45331225delinsTCCTCCT , CM000663.2:g.45331219_45331225delinsTCCTCCT GRCh38
NC_000001.10:g.45796891_45796897delinsTCCTCCT , CM000663.1:g.45796891_45796897delinsTCCTCCT GRCh37
NC_000001.9:g.45569478_45569484delinsTCCTCCT NCBI36
NG_008189.1:g.14246_14252delinsAGGAGGA , LRG_220:g.14246_14252delinsAGGAGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000412971.6:c.965_971delinsAGGAGGA ENSP00000410263.2:p.Gln322=
ENST00000435155.2:c.1382_1388delinsAGGAGGA ENSP00000403655.2:p.Gln461=
ENST00000467459.6:c.*211_*217delinsAGGAGGA ENSP00000435889.2:n.*211_*217delinsAGGAGGA
ENST00000483127.2:c.1367_1373delinsAGGAGGA ENSP00000436469.2:p.Gln456=
ENST00000485271.6:c.1349_1355delinsAGGAGGA ENSP00000431264.2:p.Gln450=
ENST00000529892.6:c.1202_1208delinsAGGAGGA ENSP00000432528.2:p.Gln401=
ENST00000533178.6:c.*678_*684delinsAGGAGGA ENSP00000436430.2:n.*678_*684delinsAGGAGGA
ENST00000672314.2:c.1349_1355delinsAGGAGGA ENSP00000500828.2:p.Gln450=
ENST00000710952.2:c.1433_1439delinsAGGAGGA MANE Plus Clinical ENSP00000518552.2:p.Gln478=
ENST00000672818.3:c.1424_1430delinsAGGAGGA ENSP00000500891.1:p.Gln475=
ENST00000456914.7:c.1349_1355delinsAGGAGGA MANE Select ENSP00000407590.2:p.Gln450=
ENST00000671898.1:c.1937_1943delinsAGGAGGA ENSP00000499896.1:p.Gln646=
ENST00000672011.1:c.*678_*684delinsAGGAGGA ENSP00000500418.1:n.*678_*684delinsAGGAGGA
ENST00000672314.1:c.1349_1355delinsAGGAGGA ENSP00000500828.1:p.Gln450=
ENST00000672818.2:c.1424_1430delinsAGGAGGA ENSP00000500891.1:p.Gln475=
ENST00000673134.1:c.*1046_*1052delinsAGGAGGA ENSP00000500526.1:n.*1046_*1052delinsAGGAGGA
ENST00000354383.10:c.1352_1358delinsAGGAGGA ENSP00000346354.6:p.Gln451=
ENST00000355498.6:c.1349_1355delinsAGGAGGA ENSP00000347685.2:p.Gln450=
ENST00000372098.7:c.1424_1430delinsAGGAGGA ENSP00000361170.3:p.Gln475=
ENST00000372104.5:c.1349_1355delinsAGGAGGA ENSP00000361176.1:p.Gln450=
ENST00000372110.7:c.1394_1400delinsAGGAGGA ENSP00000361182.3:p.Gln465=
ENST00000372115.7:c.1391_1397delinsAGGAGGA ENSP00000361187.3:p.Gln464=
ENST00000448481.5:c.1382_1388delinsAGGAGGA ENSP00000409718.1:p.Gln461=
ENST00000450313.5:c.1433_1439delinsAGGAGGA ENSP00000408176.1:p.Gln478=
ENST00000456914.6:c.1349_1355delinsAGGAGGA ENSP00000407590.2:p.Gln450=
ENST00000467459.5:c.766_772delinsAGGAGGA ENSP00000435889.1:n.766_772delinsAGGAGGA
ENST00000475516.5:c.*1162_*1168delinsAGGAGGA ENSP00000433843.1:n.*1162_*1168delinsAGGAGGA
ENST00000481571.5:c.*1162_*1168delinsAGGAGGA ENSP00000436597.1:n.*1162_*1168delinsAGGAGGA
ENST00000482094.5:n.670_676delinsAGGAGGA
ENST00000485271.5:c.46_52delinsAGGAGGA
ENST00000488731.6:c.434_440delinsAGGAGGA ENSP00000432330.1:p.Gln145=
ENST00000528013.6:c.1391_1397delinsAGGAGGA ENSP00000433130.2:p.Gln464=
ENST00000529892.5:c.424_430delinsAGGAGGA
ENST00000529984.5:c.434_440delinsAGGAGGA ENSP00000437093.1:p.Gln145=
ENST00000531105.5:c.116-1788_116-1782delinsAGGAGGA ENSP00000431292.1:n.116-1788_116-1782delinsAGGAGGA
ENST00000533178.5:c.978_984delinsAGGAGGA ENSP00000436430.1:n.978_984delinsAGGAGGA
NM_001048171.1:c.1391_1397delinsAGGAGGA NP_001041636.1:p.Gln464=
NM_001048172.1:c.1352_1358delinsAGGAGGA NP_001041637.1:p.Gln451=
NM_001048173.1:c.1349_1355delinsAGGAGGA NP_001041638.1:p.Gln450=
NM_001048174.1:c.1349_1355delinsAGGAGGA NP_001041639.1:p.Gln450=
NM_001128425.1:c.1433_1439delinsAGGAGGA , LRG_220t1:c.1433_1439delinsAGGAGGA NP_001121897.1:p.Gln478=
NM_001293190.1:c.1394_1400delinsAGGAGGA NP_001280119.1:p.Gln465=
NM_001293191.1:c.1382_1388delinsAGGAGGA NP_001280120.1:p.Gln461=
NM_001293192.1:c.1073_1079delinsAGGAGGA NP_001280121.1:p.Gln358=
NM_001293195.1:c.1349_1355delinsAGGAGGA NP_001280124.1:p.Gln450=
NM_001293196.1:c.1073_1079delinsAGGAGGA NP_001280125.1:p.Gln358=
NM_012222.2:c.1424_1430delinsAGGAGGA NP_036354.1:p.Gln475=
XM_011541497.1:c.1409_1415delinsAGGAGGA XP_011539799.1:p.Gln470=
XM_011541498.1:c.1391_1397delinsAGGAGGA XP_011539800.1:p.Gln464=
XM_011541499.1:c.1391_1397delinsAGGAGGA XP_011539801.1:p.Gln464=
XM_011541500.1:c.1391_1397delinsAGGAGGA XP_011539802.1:p.Gln464=
XM_011541501.1:c.1391_1397delinsAGGAGGA XP_011539803.1:p.Gln464=
XM_011541502.1:c.1391_1397delinsAGGAGGA XP_011539804.1:p.Gln464=
XM_011541503.1:c.1391_1397delinsAGGAGGA XP_011539805.1:p.Gln464=
XM_011541504.1:c.1382_1388delinsAGGAGGA XP_011539806.1:p.Gln461=
XM_011541505.1:c.971_977delinsAGGAGGA XP_011539807.1:p.Gln324=
XM_011541506.1:c.971_977delinsAGGAGGA XP_011539808.1:p.Gln324=
XM_011541507.1:c.962_968delinsAGGAGGA XP_011539809.1:p.Gln321=
XM_011541508.1:c.977_983delinsAGGAGGA XP_011539810.1:p.Gln326=
XR_946658.1:n.1480_1486delinsAGGAGGA
NM_001350650.1:c.1004_1010delinsAGGAGGA NP_001337579.1:p.Gln335=
NM_001350651.1:c.1004_1010delinsAGGAGGA NP_001337580.1:p.Gln335=
NR_146882.1:n.1607_1613delinsAGGAGGA
NR_146883.1:n.1421_1427delinsAGGAGGA
XM_011541497.3:c.1409_1415delinsAGGAGGA XP_011539799.1:p.Gln470=
XM_011541500.3:c.1391_1397delinsAGGAGGA XP_011539802.1:p.Gln464=
XM_011541501.2:c.1391_1397delinsAGGAGGA XP_011539803.1:p.Gln464=
XM_011541502.2:c.1391_1397delinsAGGAGGA XP_011539804.1:p.Gln464=
XM_011541503.2:c.1391_1397delinsAGGAGGA XP_011539805.1:p.Gln464=
XM_011541504.2:c.1382_1388delinsAGGAGGA XP_011539806.1:p.Gln461=
XM_011541505.2:c.971_977delinsAGGAGGA XP_011539807.1:p.Gln324=
XM_011541506.2:c.971_977delinsAGGAGGA XP_011539808.1:p.Gln324=
XM_017001331.1:c.1391_1397delinsAGGAGGA XP_016856820.1:p.Gln464=
XM_017001332.1:c.1391_1397delinsAGGAGGA XP_016856821.1:p.Gln464=
XM_017001333.1:c.1391_1397delinsAGGAGGA XP_016856822.1:p.Gln464=
XM_017001334.1:c.1352_1358delinsAGGAGGA XP_016856823.1:p.Gln451=
XM_017001335.1:c.1073_1079delinsAGGAGGA XP_016856824.1:p.Gln358=
XM_017001336.1:c.1004_1010delinsAGGAGGA XP_016856825.1:p.Gln335=
XM_017001337.1:c.1004_1010delinsAGGAGGA XP_016856826.1:p.Gln335=
XM_024447244.1:c.1004_1010delinsAGGAGGA XP_024303012.1:p.Gln335=
XM_024447245.1:c.1004_1010delinsAGGAGGA XP_024303013.1:p.Gln335=
XM_024447248.1:c.962_968delinsAGGAGGA XP_024303016.1:p.Gln321=
XM_024447249.1:c.833_839delinsAGGAGGA XP_024303017.1:p.Gln278=
XM_024447250.1:c.833_839delinsAGGAGGA XP_024303018.1:p.Gln278=
XM_024447251.1:c.833_839delinsAGGAGGA XP_024303019.1:p.Gln278=
XR_001737190.1:n.1394_1400delinsAGGAGGA
XR_001737192.1:n.1206_1212delinsAGGAGGA
XR_002956643.1:n.1386_1392delinsAGGAGGA
XR_002956644.1:n.1921_1927delinsAGGAGGA
XR_946658.2:n.1494_1500delinsAGGAGGA
NM_001048171.2:c.1349_1355delinsAGGAGGA NP_001041636.2:p.Gln450=
NM_001128425.2:c.1433_1439delinsAGGAGGA MANE Plus Clinical NP_001121897.1:p.Gln478=
NM_001048172.2:c.1352_1358delinsAGGAGGA NP_001041637.1:p.Gln451=
NM_001048173.2:c.1349_1355delinsAGGAGGA NP_001041638.1:p.Gln450=
NM_001048174.2:c.1349_1355delinsAGGAGGA MANE Select NP_001041639.1:p.Gln450=
NM_001293190.2:c.1394_1400delinsAGGAGGA NP_001280119.1:p.Gln465=
NM_001293191.2:c.1382_1388delinsAGGAGGA NP_001280120.1:p.Gln461=
NM_001293192.2:c.1073_1079delinsAGGAGGA NP_001280121.1:p.Gln358=
NM_001293195.2:c.1349_1355delinsAGGAGGA NP_001280124.1:p.Gln450=
NM_001293196.2:c.1073_1079delinsAGGAGGA NP_001280125.1:p.Gln358=
NM_001350650.2:c.1004_1010delinsAGGAGGA NP_001337579.1:p.Gln335=
NM_001350651.2:c.1004_1010delinsAGGAGGA NP_001337580.1:p.Gln335=
NM_012222.3:c.1424_1430delinsAGGAGGA NP_036354.1:p.Gln475=
NR_146882.2:n.1577_1583delinsAGGAGGA
NR_146883.2:n.1426_1432delinsAGGAGGA