Canonical Allele Identifier: CA013929
Gene: MUTYH HGNC NCBI

Linked Data

ClinVar Variation Id: 141306
dbSNP Id: rs587781645

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45332676C>G , CM000663.2:g.45332676C>G GRCh38
NC_000001.10:g.45798348C>G , CM000663.1:g.45798348C>G GRCh37
NC_000001.9:g.45570935C>G NCBI36
NG_008189.1:g.12795G>C , LRG_220:g.12795G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000450313.6:c.514G>C ENSP00000408176.2:p.Ala172Pro
ENST00000456914.7:c.504G>C MANE Select ENSP00000407590.2:p.Glu168Asp
ENST00000461495.6:c.*243G>C ENSP00000437166.1:p.=
ENST00000671856.1:n.450G>C
ENST00000671898.1:c.1092G>C ENSP00000499896.1:p.Glu364Asp
ENST00000672011.1:c.472G>C ENSP00000500418.1:p.Ala158Pro
ENST00000672314.1:c.504G>C ENSP00000500828.1:p.Glu168Asp
ENST00000672593.1:c.*392G>C ENSP00000500455.1:p.=
ENST00000672764.1:c.463G>C ENSP00000500886.1:p.Ala155Pro
ENST00000672818.2:c.579G>C ENSP00000500891.1:p.Glu193Asp
ENST00000673134.1:c.*201G>C ENSP00000500526.1:p.=
ENST00000674679.1:n.532G>C ENSP00000501623.1:p.=
ENST00000354383.10:c.507G>C ENSP00000346354.6:p.Glu169Asp
ENST00000355498.6:c.504G>C ENSP00000347685.2:p.Glu168Asp
ENST00000372098.7:c.579G>C ENSP00000361170.3:p.Glu193Asp
ENST00000372104.5:c.504G>C ENSP00000361176.1:p.Glu168Asp
ENST00000372110.7:c.549G>C ENSP00000361182.3:p.Glu183Asp
ENST00000372115.7:c.546G>C ENSP00000361187.3:p.Glu182Asp
ENST00000412971.5:c.120G>C ENSP00000410263.1:p.Glu40Asp
ENST00000435155.1:c.537G>C ENSP00000403655.1:p.Glu179Asp
ENST00000448481.5:c.537G>C ENSP00000409718.1:p.Glu179Asp
ENST00000450313.5:c.588G>C ENSP00000408176.1:p.Glu196Asp
ENST00000456914.6:c.504G>C ENSP00000407590.2:p.Glu168Asp
ENST00000461495.5:c.*243G>C ENSP00000437166.1:p.=
ENST00000462388.5:n.195G>C
ENST00000467940.5:c.*427G>C ENSP00000436478.1:p.=
ENST00000470256.5:c.391G>C ENSP00000434985.1:p.Ala131Pro
ENST00000475516.5:c.*317G>C ENSP00000433843.1:p.=
ENST00000478796.5:n.491G>C
ENST00000479746.6:n.862G>C
ENST00000481571.5:c.*317G>C ENSP00000436597.1:p.=
ENST00000483642.5:n.1019G>C
ENST00000488731.6:c.187+87G>C ENSP00000432330.1:p.=
ENST00000492494.5:n.901G>C
ENST00000525160.5:c.*155G>C ENSP00000431568.1:p.=
ENST00000528013.6:c.546G>C ENSP00000433130.2:p.Glu182Asp
ENST00000529984.5:c.187+87G>C ENSP00000437093.1:p.=
ENST00000531105.5:c.115+1715G>C ENSP00000431292.1:p.=
ENST00000533178.5:n.133G>C ENSP00000436430.1:p.Ala45Pro
NM_001048171.1:c.546G>C NP_001041636.1:p.Glu182Asp
NM_001048172.1:c.507G>C NP_001041637.1:p.Glu169Asp
NM_001048173.1:c.504G>C NP_001041638.1:p.Glu168Asp
NM_001048174.1:c.504G>C NP_001041639.1:p.Glu168Asp
NM_001128425.1:c.588G>C , LRG_220t1:c.588G>C NP_001121897.1:p.Glu196Asp
NM_001293190.1:c.549G>C NP_001280119.1:p.Glu183Asp
NM_001293191.1:c.537G>C NP_001280120.1:p.Glu179Asp
NM_001293192.1:c.228G>C NP_001280121.1:p.Glu76Asp
NM_001293195.1:c.504G>C NP_001280124.1:p.Glu168Asp
NM_001293196.1:c.228G>C NP_001280125.1:p.Glu76Asp
NM_012222.2:c.579G>C NP_036354.1:p.Glu193Asp
XM_011541497.1:c.564G>C XP_011539799.1:p.Glu188Asp
XM_011541498.1:c.546G>C XP_011539800.1:p.Glu182Asp
XM_011541499.1:c.546G>C XP_011539801.1:p.Glu182Asp
XM_011541500.1:c.546G>C XP_011539802.1:p.Glu182Asp
XM_011541501.1:c.546G>C XP_011539803.1:p.Glu182Asp
XM_011541502.1:c.546G>C XP_011539804.1:p.Glu182Asp
XM_011541503.1:c.546G>C XP_011539805.1:p.Glu182Asp
XM_011541504.1:c.537G>C XP_011539806.1:p.Glu179Asp
XM_011541505.1:c.126G>C XP_011539807.1:p.Glu42Asp
XM_011541506.1:c.126G>C XP_011539808.1:p.Glu42Asp
XM_011541507.1:c.117G>C XP_011539809.1:p.Glu39Asp
XM_011541508.1:c.132G>C XP_011539810.1:p.Glu44Asp
XR_946658.1:n.635G>C
NM_001350650.1:c.159G>C NP_001337579.1:p.Glu53Asp
NM_001350651.1:c.159G>C NP_001337580.1:p.Glu53Asp
NR_146882.1:n.762G>C
NR_146883.1:n.576G>C
XM_011541497.3:c.564G>C XP_011539799.1:p.Glu188Asp
XM_011541500.3:c.546G>C XP_011539802.1:p.Glu182Asp
XM_011541501.2:c.546G>C XP_011539803.1:p.Glu182Asp
XM_011541502.2:c.546G>C XP_011539804.1:p.Glu182Asp
XM_011541503.2:c.546G>C XP_011539805.1:p.Glu182Asp
XM_011541504.2:c.537G>C XP_011539806.1:p.Glu179Asp
XM_011541505.2:c.126G>C XP_011539807.1:p.Glu42Asp
XM_011541506.2:c.126G>C XP_011539808.1:p.Glu42Asp
XM_017001331.1:c.546G>C XP_016856820.1:p.Glu182Asp
XM_017001332.1:c.546G>C XP_016856821.1:p.Glu182Asp
XM_017001333.1:c.546G>C XP_016856822.1:p.Glu182Asp
XM_017001334.1:c.507G>C XP_016856823.1:p.Glu169Asp
XM_017001335.1:c.228G>C XP_016856824.1:p.Glu76Asp
XM_017001336.1:c.159G>C XP_016856825.1:p.Glu53Asp
XM_017001337.1:c.159G>C XP_016856826.1:p.Glu53Asp
XM_024447244.1:c.159G>C XP_024303012.1:p.Glu53Asp
XM_024447245.1:c.159G>C XP_024303013.1:p.Glu53Asp
XM_024447248.1:c.117G>C XP_024303016.1:p.Glu39Asp
XM_024447249.1:c.-13G>C XP_024303017.1:p.=
XM_024447250.1:c.-13G>C XP_024303018.1:p.=
XM_024447251.1:c.-13G>C XP_024303019.1:p.=
XR_001737190.1:n.549G>C
XR_001737192.1:n.361G>C
XR_002956643.1:n.541G>C
XR_002956644.1:n.1076G>C
XR_946658.2:n.649G>C
NM_001048171.2:c.504G>C NP_001041636.2:p.Glu168Asp
NM_001128425.2:c.588G>C NP_001121897.1:p.Glu196Asp
NM_001048172.2:c.507G>C NP_001041637.1:p.Glu169Asp
NM_001048173.2:c.504G>C NP_001041638.1:p.Glu168Asp
NM_001048174.2:c.504G>C MANE Select NP_001041639.1:p.Glu168Asp
NM_001293190.2:c.549G>C NP_001280119.1:p.Glu183Asp
NM_001293191.2:c.537G>C NP_001280120.1:p.Glu179Asp
NM_001293192.2:c.228G>C NP_001280121.1:p.Glu76Asp
NM_001293195.2:c.504G>C NP_001280124.1:p.Glu168Asp
NM_001293196.2:c.228G>C NP_001280125.1:p.Glu76Asp
NM_001350650.2:c.159G>C NP_001337579.1:p.Glu53Asp
NM_001350651.2:c.159G>C NP_001337580.1:p.Glu53Asp
NM_012222.3:c.579G>C NP_036354.1:p.Glu193Asp
NR_146882.2:n.732G>C
NR_146883.2:n.581G>C