Canonical Allele Identifier: CA1001243563
Gene: MUTYH HGNC NCBI

Linked Data

dbSNP Id: rs1644777520

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45331252_45331259del , CM000663.2:g.45331252_45331259del GRCh38
NC_000001.10:g.45796924_45796931del , CM000663.1:g.45796924_45796931del GRCh37
NC_000001.9:g.45569511_45569518del NCBI36
NG_008189.1:g.14218_14225del , LRG_220:g.14218_14225del

Transcript Alleles

HGVS Amino-acid change
ENST00000412971.6:c.937_944del ENSP00000410263.2:p.Val313ArgfsTer?
ENST00000435155.2:c.1354_1361del ENSP00000403655.2:p.Val452ArgfsTer?
ENST00000467459.6:c.*183_*190del ENSP00000435889.2:n.*183_*190del
ENST00000483127.2:c.1339_1346del ENSP00000436469.2:p.Val447ArgfsTer?
ENST00000485271.6:c.1321_1328del ENSP00000431264.2:p.Val441ArgfsTer?
ENST00000529892.6:c.1174_1181del ENSP00000432528.2:p.Val392ArgfsTer?
ENST00000533178.6:c.*650_*657del ENSP00000436430.2:n.*650_*657del
ENST00000672314.2:c.1321_1328del ENSP00000500828.2:p.Val441ArgfsTer?
ENST00000710952.2:c.1405_1412del MANE Plus Clinical ENSP00000518552.2:p.Val469ArgfsTer?
ENST00000672818.3:c.1396_1403del ENSP00000500891.1:p.Val466ArgfsTer?
ENST00000456914.7:c.1321_1328del MANE Select ENSP00000407590.2:p.Val441ArgfsTer?
ENST00000671898.1:c.1909_1916del ENSP00000499896.1:p.Val637ArgfsTer?
ENST00000672011.1:c.*650_*657del ENSP00000500418.1:n.*650_*657del
ENST00000672314.1:c.1321_1328del ENSP00000500828.1:p.Val441ArgfsTer?
ENST00000672818.2:c.1396_1403del ENSP00000500891.1:p.Val466ArgfsTer?
ENST00000673134.1:c.*1018_*1025del ENSP00000500526.1:n.*1018_*1025del
ENST00000354383.10:c.1324_1331del ENSP00000346354.6:p.Val442ArgfsTer?
ENST00000355498.6:c.1321_1328del ENSP00000347685.2:p.Val441ArgfsTer?
ENST00000372098.7:c.1396_1403del ENSP00000361170.3:p.Val466ArgfsTer?
ENST00000372104.5:c.1321_1328del ENSP00000361176.1:p.Val441ArgfsTer?
ENST00000372110.7:c.1366_1373del ENSP00000361182.3:p.Val456ArgfsTer?
ENST00000372115.7:c.1363_1370del ENSP00000361187.3:p.Val455ArgfsTer?
ENST00000448481.5:c.1354_1361del ENSP00000409718.1:p.Val452ArgfsTer?
ENST00000450313.5:c.1405_1412del ENSP00000408176.1:p.Val469ArgfsTer?
ENST00000456914.6:c.1321_1328del ENSP00000407590.2:p.Val441ArgfsTer?
ENST00000467459.5:c.738_745del ENSP00000435889.1:n.738_745del
ENST00000475516.5:c.*1134_*1141del ENSP00000433843.1:n.*1134_*1141del
ENST00000481571.5:c.*1134_*1141del ENSP00000436597.1:n.*1134_*1141del
ENST00000482094.5:n.642_649del
ENST00000485271.5:c.18_25del
ENST00000488731.6:c.406_413del ENSP00000432330.1:p.Val136ArgfsTer?
ENST00000528013.6:c.1363_1370del ENSP00000433130.2:p.Val455ArgfsTer?
ENST00000529892.5:c.396_403del
ENST00000529984.5:c.406_413del ENSP00000437093.1:p.Val136ArgfsTer?
ENST00000531105.5:c.116-1816_116-1809del ENSP00000431292.1:n.116-1816_116-1809del
ENST00000533178.5:c.950_957del ENSP00000436430.1:n.950_957del
NM_001048171.1:c.1363_1370del NP_001041636.1:p.Val455ArgfsTer?
NM_001048172.1:c.1324_1331del NP_001041637.1:p.Val442ArgfsTer?
NM_001048173.1:c.1321_1328del NP_001041638.1:p.Val441ArgfsTer?
NM_001048174.1:c.1321_1328del NP_001041639.1:p.Val441ArgfsTer?
NM_001128425.1:c.1405_1412del , LRG_220t1:c.1405_1412del NP_001121897.1:p.Val469ArgfsTer?
NM_001293190.1:c.1366_1373del NP_001280119.1:p.Val456ArgfsTer?
NM_001293191.1:c.1354_1361del NP_001280120.1:p.Val452ArgfsTer?
NM_001293192.1:c.1045_1052del NP_001280121.1:p.Val349ArgfsTer?
NM_001293195.1:c.1321_1328del NP_001280124.1:p.Val441ArgfsTer?
NM_001293196.1:c.1045_1052del NP_001280125.1:p.Val349ArgfsTer?
NM_012222.2:c.1396_1403del NP_036354.1:p.Val466ArgfsTer?
XM_011541497.1:c.1381_1388del XP_011539799.1:p.Val461ArgfsTer?
XM_011541498.1:c.1363_1370del XP_011539800.1:p.Val455ArgfsTer?
XM_011541499.1:c.1363_1370del XP_011539801.1:p.Val455ArgfsTer?
XM_011541500.1:c.1363_1370del XP_011539802.1:p.Val455ArgfsTer?
XM_011541501.1:c.1363_1370del XP_011539803.1:p.Val455ArgfsTer?
XM_011541502.1:c.1363_1370del XP_011539804.1:p.Val455ArgfsTer?
XM_011541503.1:c.1363_1370del XP_011539805.1:p.Val455ArgfsTer?
XM_011541504.1:c.1354_1361del XP_011539806.1:p.Val452ArgfsTer?
XM_011541505.1:c.943_950del XP_011539807.1:p.Val315ArgfsTer?
XM_011541506.1:c.943_950del XP_011539808.1:p.Val315ArgfsTer?
XM_011541507.1:c.934_941del XP_011539809.1:p.Val312ArgfsTer?
XM_011541508.1:c.949_956del XP_011539810.1:p.Val317ArgfsTer?
XR_946658.1:n.1452_1459del
NM_001350650.1:c.976_983del NP_001337579.1:p.Val326ArgfsTer?
NM_001350651.1:c.976_983del NP_001337580.1:p.Val326ArgfsTer?
NR_146882.1:n.1579_1586del
NR_146883.1:n.1393_1400del
XM_011541497.3:c.1381_1388del XP_011539799.1:p.Val461ArgfsTer?
XM_011541500.3:c.1363_1370del XP_011539802.1:p.Val455ArgfsTer?
XM_011541501.2:c.1363_1370del XP_011539803.1:p.Val455ArgfsTer?
XM_011541502.2:c.1363_1370del XP_011539804.1:p.Val455ArgfsTer?
XM_011541503.2:c.1363_1370del XP_011539805.1:p.Val455ArgfsTer?
XM_011541504.2:c.1354_1361del XP_011539806.1:p.Val452ArgfsTer?
XM_011541505.2:c.943_950del XP_011539807.1:p.Val315ArgfsTer?
XM_011541506.2:c.943_950del XP_011539808.1:p.Val315ArgfsTer?
XM_017001331.1:c.1363_1370del XP_016856820.1:p.Val455ArgfsTer?
XM_017001332.1:c.1363_1370del XP_016856821.1:p.Val455ArgfsTer?
XM_017001333.1:c.1363_1370del XP_016856822.1:p.Val455ArgfsTer?
XM_017001334.1:c.1324_1331del XP_016856823.1:p.Val442ArgfsTer?
XM_017001335.1:c.1045_1052del XP_016856824.1:p.Val349ArgfsTer?
XM_017001336.1:c.976_983del XP_016856825.1:p.Val326ArgfsTer?
XM_017001337.1:c.976_983del XP_016856826.1:p.Val326ArgfsTer?
XM_024447244.1:c.976_983del XP_024303012.1:p.Val326ArgfsTer?
XM_024447245.1:c.976_983del XP_024303013.1:p.Val326ArgfsTer?
XM_024447248.1:c.934_941del XP_024303016.1:p.Val312ArgfsTer?
XM_024447249.1:c.805_812del XP_024303017.1:p.Val269ArgfsTer?
XM_024447250.1:c.805_812del XP_024303018.1:p.Val269ArgfsTer?
XM_024447251.1:c.805_812del XP_024303019.1:p.Val269ArgfsTer?
XR_001737190.1:n.1366_1373del
XR_001737192.1:n.1178_1185del
XR_002956643.1:n.1358_1365del
XR_002956644.1:n.1893_1900del
XR_946658.2:n.1466_1473del
NM_001048171.2:c.1321_1328del NP_001041636.2:p.Val441ArgfsTer?
NM_001128425.2:c.1405_1412del MANE Plus Clinical NP_001121897.1:p.Val469ArgfsTer?
NM_001048172.2:c.1324_1331del NP_001041637.1:p.Val442ArgfsTer?
NM_001048173.2:c.1321_1328del NP_001041638.1:p.Val441ArgfsTer?
NM_001048174.2:c.1321_1328del MANE Select NP_001041639.1:p.Val441ArgfsTer?
NM_001293190.2:c.1366_1373del NP_001280119.1:p.Val456ArgfsTer?
NM_001293191.2:c.1354_1361del NP_001280120.1:p.Val452ArgfsTer?
NM_001293192.2:c.1045_1052del NP_001280121.1:p.Val349ArgfsTer?
NM_001293195.2:c.1321_1328del NP_001280124.1:p.Val441ArgfsTer?
NM_001293196.2:c.1045_1052del NP_001280125.1:p.Val349ArgfsTer?
NM_001350650.2:c.976_983del NP_001337579.1:p.Val326ArgfsTer?
NM_001350651.2:c.976_983del NP_001337580.1:p.Val326ArgfsTer?
NM_012222.3:c.1396_1403del NP_036354.1:p.Val466ArgfsTer?
NR_146882.2:n.1549_1556del
NR_146883.2:n.1398_1405del