Canonical Allele Identifier: CA340135925
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 1492882
ClinVar RCV Id: RCV001983945
dbSNP Id: rs2149160813

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45332928G>A , CM000663.2:g.45332928G>A GRCh38
NC_000001.10:g.45798600G>A , CM000663.1:g.45798600G>A GRCh37
NC_000001.9:g.45571187G>A NCBI36
NG_008189.1:g.12543C>T , LRG_220:g.12543C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000412971.6:c.37-94C>T ENSP00000410263.2:n.37-94C>T
ENST00000435155.2:c.443C>T ENSP00000403655.2:p.Ala148Val
ENST00000467459.6:c.410C>T ENSP00000435889.2:p.Ala137Val
ENST00000483127.2:c.428C>T ENSP00000436469.2:p.Ala143Val
ENST00000485271.6:c.410C>T ENSP00000431264.2:p.Ala137Val
ENST00000529892.6:c.452C>T ENSP00000432528.2:p.Ala151Val
ENST00000533178.6:c.116-241C>T ENSP00000436430.2:n.116-241C>T
ENST00000672314.2:c.410C>T ENSP00000500828.2:p.Ala137Val
ENST00000674679.2:c.*322C>T ENSP00000501623.2:n.*322C>T
ENST00000710952.2:c.494C>T MANE Plus Clinical ENSP00000518552.2:p.Ala165Val
ENST00000672818.3:c.485C>T ENSP00000500891.1:p.Ala162Val
ENST00000450313.6:c.420C>T ENSP00000408176.2:p.Cys140=
ENST00000456914.7:c.410C>T MANE Select ENSP00000407590.2:p.Ala137Val
ENST00000461495.6:c.*149C>T ENSP00000437166.1:n.*149C>T
ENST00000671856.1:n.356C>T
ENST00000671898.1:c.998C>T ENSP00000499896.1:p.Ala333Val
ENST00000672011.1:c.378C>T ENSP00000500418.1:p.Cys126=
ENST00000672314.1:c.410C>T ENSP00000500828.1:p.Ala137Val
ENST00000672593.1:c.*223C>T ENSP00000500455.1:n.*223C>T
ENST00000672764.1:c.369C>T ENSP00000500886.1:p.Cys123=
ENST00000672818.2:c.485C>T ENSP00000500891.1:p.Ala162Val
ENST00000673134.1:c.*118-94C>T ENSP00000500526.1:n.*118-94C>T
ENST00000674679.1:c.438C>T ENSP00000501623.1:n.438C>T
ENST00000354383.10:c.413C>T ENSP00000346354.6:p.Ala138Val
ENST00000355498.6:c.410C>T ENSP00000347685.2:p.Ala137Val
ENST00000372098.7:c.485C>T ENSP00000361170.3:p.Ala162Val
ENST00000372104.5:c.410C>T ENSP00000361176.1:p.Ala137Val
ENST00000372110.7:c.455C>T ENSP00000361182.3:p.Ala152Val
ENST00000372115.7:c.452C>T ENSP00000361187.3:p.Ala151Val
ENST00000412971.5:c.37-94C>T ENSP00000410263.1:n.37-94C>T
ENST00000435155.1:c.443C>T ENSP00000403655.1:p.Ala148Val
ENST00000448481.5:c.443C>T ENSP00000409718.1:p.Ala148Val
ENST00000450313.5:c.494C>T ENSP00000408176.1:p.Ala165Val
ENST00000456914.6:c.410C>T ENSP00000407590.2:p.Ala137Val
ENST00000461495.5:c.*149C>T ENSP00000437166.1:n.*149C>T
ENST00000462387.5:n.732C>T
ENST00000462388.5:n.18C>T
ENST00000467940.5:c.*333C>T ENSP00000436478.1:n.*333C>T
ENST00000470256.5:c.308-94C>T ENSP00000434985.1:n.308-94C>T
ENST00000475516.5:c.*223C>T ENSP00000433843.1:n.*223C>T
ENST00000476789.5:n.767C>T
ENST00000478796.5:n.397C>T
ENST00000479746.6:n.610C>T
ENST00000481139.5:n.800C>T
ENST00000481571.5:c.*223C>T ENSP00000436597.1:n.*223C>T
ENST00000483642.5:n.842C>T
ENST00000485484.5:n.711C>T
ENST00000488731.6:c.116-94C>T ENSP00000432330.1:n.116-94C>T
ENST00000492494.5:n.724C>T
ENST00000525160.5:c.*61C>T ENSP00000431568.1:n.*61C>T
ENST00000528013.6:c.452C>T ENSP00000433130.2:p.Ala151Val
ENST00000529984.5:c.116-94C>T ENSP00000437093.1:n.116-94C>T
ENST00000531105.5:c.115+1463C>T ENSP00000431292.1:n.115+1463C>T
ENST00000533178.5:c.122-241C>T ENSP00000436430.1:n.122-241C>T
NM_001048171.1:c.452C>T NP_001041636.1:p.Ala151Val
NM_001048172.1:c.413C>T NP_001041637.1:p.Ala138Val
NM_001048173.1:c.410C>T NP_001041638.1:p.Ala137Val
NM_001048174.1:c.410C>T NP_001041639.1:p.Ala137Val
NM_001128425.1:c.494C>T , LRG_220t1:c.494C>T NP_001121897.1:p.Ala165Val
NM_001293190.1:c.455C>T NP_001280119.1:p.Ala152Val
NM_001293191.1:c.443C>T NP_001280120.1:p.Ala148Val
NM_001293192.1:c.134C>T NP_001280121.1:p.Ala45Val
NM_001293195.1:c.410C>T NP_001280124.1:p.Ala137Val
NM_001293196.1:c.134C>T NP_001280125.1:p.Ala45Val
NM_012222.2:c.485C>T NP_036354.1:p.Ala162Val
XM_011541497.1:c.470C>T XP_011539799.1:p.Ala157Val
XM_011541498.1:c.452C>T XP_011539800.1:p.Ala151Val
XM_011541499.1:c.452C>T XP_011539801.1:p.Ala151Val
XM_011541500.1:c.452C>T XP_011539802.1:p.Ala151Val
XM_011541501.1:c.452C>T XP_011539803.1:p.Ala151Val
XM_011541502.1:c.452C>T XP_011539804.1:p.Ala151Val
XM_011541503.1:c.463-94C>T XP_011539805.1:n.463-94C>T
XM_011541504.1:c.443C>T XP_011539806.1:p.Ala148Val
XM_011541505.1:c.43-94C>T XP_011539807.1:n.43-94C>T
XM_011541506.1:c.43-94C>T XP_011539808.1:n.43-94C>T
XM_011541507.1:c.34-94C>T XP_011539809.1:n.34-94C>T
XM_011541508.1:c.38C>T XP_011539810.1:p.Ala13Val
XR_946658.1:n.541C>T
NM_001350650.1:c.65C>T NP_001337579.1:p.Ala22Val
NM_001350651.1:c.65C>T NP_001337580.1:p.Ala22Val
NR_146882.1:n.668C>T
NR_146883.1:n.482C>T
XM_011541497.3:c.470C>T XP_011539799.1:p.Ala157Val
XM_011541500.3:c.452C>T XP_011539802.1:p.Ala151Val
XM_011541501.2:c.452C>T XP_011539803.1:p.Ala151Val
XM_011541502.2:c.452C>T XP_011539804.1:p.Ala151Val
XM_011541503.2:c.463-94C>T XP_011539805.1:n.463-94C>T
XM_011541504.2:c.443C>T XP_011539806.1:p.Ala148Val
XM_011541505.2:c.43-94C>T XP_011539807.1:n.43-94C>T
XM_011541506.2:c.43-94C>T XP_011539808.1:n.43-94C>T
XM_017001331.1:c.452C>T XP_016856820.1:p.Ala151Val
XM_017001332.1:c.452C>T XP_016856821.1:p.Ala151Val
XM_017001333.1:c.452C>T XP_016856822.1:p.Ala151Val
XM_017001334.1:c.413C>T XP_016856823.1:p.Ala138Val
XM_017001335.1:c.134C>T XP_016856824.1:p.Ala45Val
XM_017001336.1:c.65C>T XP_016856825.1:p.Ala22Val
XM_017001337.1:c.65C>T XP_016856826.1:p.Ala22Val
XM_024447244.1:c.65C>T XP_024303012.1:p.Ala22Val
XM_024447245.1:c.65C>T XP_024303013.1:p.Ala22Val
XM_024447248.1:c.34-94C>T XP_024303016.1:n.34-94C>T
XM_024447249.1:c.-107C>T XP_024303017.1:n.-107C>T
XM_024447250.1:c.-107C>T XP_024303018.1:n.-107C>T
XM_024447251.1:c.-190C>T XP_024303019.1:n.-190C>T
XR_001737190.1:n.455C>T
XR_001737192.1:n.278-94C>T
XR_002956643.1:n.458-94C>T
XR_002956644.1:n.899C>T
XR_946658.2:n.555C>T
NM_001048171.2:c.410C>T NP_001041636.2:p.Ala137Val
NM_001128425.2:c.494C>T MANE Plus Clinical NP_001121897.1:p.Ala165Val
NM_001048172.2:c.413C>T NP_001041637.1:p.Ala138Val
NM_001048173.2:c.410C>T NP_001041638.1:p.Ala137Val
NM_001048174.2:c.410C>T MANE Select NP_001041639.1:p.Ala137Val
NM_001293190.2:c.455C>T NP_001280119.1:p.Ala152Val
NM_001293191.2:c.443C>T NP_001280120.1:p.Ala148Val
NM_001293192.2:c.134C>T NP_001280121.1:p.Ala45Val
NM_001293195.2:c.410C>T NP_001280124.1:p.Ala137Val
NM_001293196.2:c.134C>T NP_001280125.1:p.Ala45Val
NM_001350650.2:c.65C>T NP_001337579.1:p.Ala22Val
NM_001350651.2:c.65C>T NP_001337580.1:p.Ala22Val
NM_012222.3:c.485C>T NP_036354.1:p.Ala162Val
NR_146882.2:n.638C>T
NR_146883.2:n.487C>T