Canonical Allele Identifier: CA2473712157
Gene: MUTYH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45331318_45331321delinsGAGA , CM000663.2:g.45331318_45331321delinsGAGA GRCh38
NC_000001.10:g.45796990_45796993delinsGAGA , CM000663.1:g.45796990_45796993delinsGAGA GRCh37
NC_000001.9:g.45569577_45569580delinsGAGA NCBI36
NG_008189.1:g.14150_14153delinsTCTC , LRG_220:g.14150_14153delinsTCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000412971.6:c.869_872delinsTCTC ENSP00000410263.2:p.Phe290=
ENST00000435155.2:c.1286_1289delinsTCTC ENSP00000403655.2:p.Phe429=
ENST00000467459.6:c.*115_*118delinsTCTC ENSP00000435889.2:n.*115_*118delinsTCTC
ENST00000483127.2:c.1271_1274delinsTCTC ENSP00000436469.2:p.Phe424=
ENST00000485271.6:c.1253_1256delinsTCTC ENSP00000431264.2:p.Phe418=
ENST00000529892.6:c.1106_1109delinsTCTC ENSP00000432528.2:p.Phe369=
ENST00000533178.6:c.*582_*585delinsTCTC ENSP00000436430.2:n.*582_*585delinsTCTC
ENST00000672314.2:c.1253_1256delinsTCTC ENSP00000500828.2:p.Phe418=
ENST00000710952.2:c.1337_1340delinsTCTC MANE Plus Clinical ENSP00000518552.2:p.Phe446=
ENST00000672818.3:c.1328_1331delinsTCTC ENSP00000500891.1:p.Phe443=
ENST00000456914.7:c.1253_1256delinsTCTC MANE Select ENSP00000407590.2:p.Phe418=
ENST00000671898.1:c.1841_1844delinsTCTC ENSP00000499896.1:p.Phe614=
ENST00000672011.1:c.*582_*585delinsTCTC ENSP00000500418.1:n.*582_*585delinsTCTC
ENST00000672314.1:c.1253_1256delinsTCTC ENSP00000500828.1:p.Phe418=
ENST00000672818.2:c.1328_1331delinsTCTC ENSP00000500891.1:p.Phe443=
ENST00000673134.1:c.*950_*953delinsTCTC ENSP00000500526.1:n.*950_*953delinsTCTC
ENST00000354383.10:c.1256_1259delinsTCTC ENSP00000346354.6:p.Phe419=
ENST00000355498.6:c.1253_1256delinsTCTC ENSP00000347685.2:p.Phe418=
ENST00000372098.7:c.1328_1331delinsTCTC ENSP00000361170.3:p.Phe443=
ENST00000372104.5:c.1253_1256delinsTCTC ENSP00000361176.1:p.Phe418=
ENST00000372110.7:c.1298_1301delinsTCTC ENSP00000361182.3:p.Phe433=
ENST00000372115.7:c.1295_1298delinsTCTC ENSP00000361187.3:p.Phe432=
ENST00000448481.5:c.1286_1289delinsTCTC ENSP00000409718.1:p.Phe429=
ENST00000450313.5:c.1337_1340delinsTCTC ENSP00000408176.1:p.Phe446=
ENST00000456914.6:c.1253_1256delinsTCTC ENSP00000407590.2:p.Phe418=
ENST00000467459.5:c.670_673delinsTCTC ENSP00000435889.1:n.670_673delinsTCTC
ENST00000475516.5:c.*1066_*1069delinsTCTC ENSP00000433843.1:n.*1066_*1069delinsTCTC
ENST00000481571.5:c.*1066_*1069delinsTCTC ENSP00000436597.1:n.*1066_*1069delinsTCTC
ENST00000482094.5:n.574_577delinsTCTC
ENST00000488731.6:c.338_341delinsTCTC ENSP00000432330.1:p.Phe113=
ENST00000528013.6:c.1295_1298delinsTCTC ENSP00000433130.2:p.Phe432=
ENST00000529892.5:c.328_331delinsTCTC
ENST00000529984.5:c.338_341delinsTCTC ENSP00000437093.1:p.Phe113=
ENST00000531105.5:c.116-1884_116-1881delinsTCTC ENSP00000431292.1:n.116-1884_116-1881delinsTCTC
ENST00000533178.5:c.882_885delinsTCTC ENSP00000436430.1:n.882_885delinsTCTC
NM_001048171.1:c.1295_1298delinsTCTC NP_001041636.1:p.Phe432=
NM_001048172.1:c.1256_1259delinsTCTC NP_001041637.1:p.Phe419=
NM_001048173.1:c.1253_1256delinsTCTC NP_001041638.1:p.Phe418=
NM_001048174.1:c.1253_1256delinsTCTC NP_001041639.1:p.Phe418=
NM_001128425.1:c.1337_1340delinsTCTC , LRG_220t1:c.1337_1340delinsTCTC NP_001121897.1:p.Phe446=
NM_001293190.1:c.1298_1301delinsTCTC NP_001280119.1:p.Phe433=
NM_001293191.1:c.1286_1289delinsTCTC NP_001280120.1:p.Phe429=
NM_001293192.1:c.977_980delinsTCTC NP_001280121.1:p.Phe326=
NM_001293195.1:c.1253_1256delinsTCTC NP_001280124.1:p.Phe418=
NM_001293196.1:c.977_980delinsTCTC NP_001280125.1:p.Phe326=
NM_012222.2:c.1328_1331delinsTCTC NP_036354.1:p.Phe443=
XM_011541497.1:c.1313_1316delinsTCTC XP_011539799.1:p.Phe438=
XM_011541498.1:c.1295_1298delinsTCTC XP_011539800.1:p.Phe432=
XM_011541499.1:c.1295_1298delinsTCTC XP_011539801.1:p.Phe432=
XM_011541500.1:c.1295_1298delinsTCTC XP_011539802.1:p.Phe432=
XM_011541501.1:c.1295_1298delinsTCTC XP_011539803.1:p.Phe432=
XM_011541502.1:c.1295_1298delinsTCTC XP_011539804.1:p.Phe432=
XM_011541503.1:c.1295_1298delinsTCTC XP_011539805.1:p.Phe432=
XM_011541504.1:c.1286_1289delinsTCTC XP_011539806.1:p.Phe429=
XM_011541505.1:c.875_878delinsTCTC XP_011539807.1:p.Phe292=
XM_011541506.1:c.875_878delinsTCTC XP_011539808.1:p.Phe292=
XM_011541507.1:c.866_869delinsTCTC XP_011539809.1:p.Phe289=
XM_011541508.1:c.881_884delinsTCTC XP_011539810.1:p.Phe294=
XR_946658.1:n.1384_1387delinsTCTC
NM_001350650.1:c.908_911delinsTCTC NP_001337579.1:p.Phe303=
NM_001350651.1:c.908_911delinsTCTC NP_001337580.1:p.Phe303=
NR_146882.1:n.1511_1514delinsTCTC
NR_146883.1:n.1325_1328delinsTCTC
XM_011541497.3:c.1313_1316delinsTCTC XP_011539799.1:p.Phe438=
XM_011541500.3:c.1295_1298delinsTCTC XP_011539802.1:p.Phe432=
XM_011541501.2:c.1295_1298delinsTCTC XP_011539803.1:p.Phe432=
XM_011541502.2:c.1295_1298delinsTCTC XP_011539804.1:p.Phe432=
XM_011541503.2:c.1295_1298delinsTCTC XP_011539805.1:p.Phe432=
XM_011541504.2:c.1286_1289delinsTCTC XP_011539806.1:p.Phe429=
XM_011541505.2:c.875_878delinsTCTC XP_011539807.1:p.Phe292=
XM_011541506.2:c.875_878delinsTCTC XP_011539808.1:p.Phe292=
XM_017001331.1:c.1295_1298delinsTCTC XP_016856820.1:p.Phe432=
XM_017001332.1:c.1295_1298delinsTCTC XP_016856821.1:p.Phe432=
XM_017001333.1:c.1295_1298delinsTCTC XP_016856822.1:p.Phe432=
XM_017001334.1:c.1256_1259delinsTCTC XP_016856823.1:p.Phe419=
XM_017001335.1:c.977_980delinsTCTC XP_016856824.1:p.Phe326=
XM_017001336.1:c.908_911delinsTCTC XP_016856825.1:p.Phe303=
XM_017001337.1:c.908_911delinsTCTC XP_016856826.1:p.Phe303=
XM_024447244.1:c.908_911delinsTCTC XP_024303012.1:p.Phe303=
XM_024447245.1:c.908_911delinsTCTC XP_024303013.1:p.Phe303=
XM_024447248.1:c.866_869delinsTCTC XP_024303016.1:p.Phe289=
XM_024447249.1:c.737_740delinsTCTC XP_024303017.1:p.Phe246=
XM_024447250.1:c.737_740delinsTCTC XP_024303018.1:p.Phe246=
XM_024447251.1:c.737_740delinsTCTC XP_024303019.1:p.Phe246=
XR_001737190.1:n.1298_1301delinsTCTC
XR_001737192.1:n.1110_1113delinsTCTC
XR_002956643.1:n.1290_1293delinsTCTC
XR_002956644.1:n.1825_1828delinsTCTC
XR_946658.2:n.1398_1401delinsTCTC
NM_001048171.2:c.1253_1256delinsTCTC NP_001041636.2:p.Phe418=
NM_001128425.2:c.1337_1340delinsTCTC MANE Plus Clinical NP_001121897.1:p.Phe446=
NM_001048172.2:c.1256_1259delinsTCTC NP_001041637.1:p.Phe419=
NM_001048173.2:c.1253_1256delinsTCTC NP_001041638.1:p.Phe418=
NM_001048174.2:c.1253_1256delinsTCTC MANE Select NP_001041639.1:p.Phe418=
NM_001293190.2:c.1298_1301delinsTCTC NP_001280119.1:p.Phe433=
NM_001293191.2:c.1286_1289delinsTCTC NP_001280120.1:p.Phe429=
NM_001293192.2:c.977_980delinsTCTC NP_001280121.1:p.Phe326=
NM_001293195.2:c.1253_1256delinsTCTC NP_001280124.1:p.Phe418=
NM_001293196.2:c.977_980delinsTCTC NP_001280125.1:p.Phe326=
NM_001350650.2:c.908_911delinsTCTC NP_001337579.1:p.Phe303=
NM_001350651.2:c.908_911delinsTCTC NP_001337580.1:p.Phe303=
NM_012222.3:c.1328_1331delinsTCTC NP_036354.1:p.Phe443=
NR_146882.2:n.1481_1484delinsTCTC
NR_146883.2:n.1330_1333delinsTCTC