Canonical Allele Identifier: CA340135450

Gene: MUTYH

Linked Data

• ClinVar Variation Id: 1006288
• ClinVar RCV Id: RCV001303307
• dbSNP Id: rs745921592
• MyVariant Identifiers: chr1:g.45798350C>G (hg19) ; chr1:g.45332678C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45332678C>G , CM000663.2:g.45332678C>G	GRCh38
NC_000001.10:g.45798350C>G , CM000663.1:g.45798350C>G	GRCh37
NC_000001.9:g.45570937C>G	NCBI36
NG_008189.1:g.12793G>C , LRG_220:g.12793G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412971.6:c.118G>C	ENSP00000410263.2:p.Glu40Gln
ENST00000435155.2:c.535G>C	ENSP00000403655.2:p.Glu179Gln
ENST00000467459.6:c.502G>C	ENSP00000435889.2:p.Glu168Gln
ENST00000483127.2:c.520G>C	ENSP00000436469.2:p.Glu174Gln
ENST00000485271.6:c.502G>C	ENSP00000431264.2:p.Glu168Gln
ENST00000529892.6:c.544G>C	ENSP00000432528.2:p.Glu182Gln
ENST00000533178.6:c.125G>C	ENSP00000436430.2:p.Gly42Ala
ENST00000672314.2:c.502G>C	ENSP00000500828.2:p.Glu168Gln
ENST00000674679.2:c.*414G>C	ENSP00000501623.2:n.*414G>C
ENST00000710952.2:c.586G>C MANE Plus Clinical	ENSP00000518552.2:p.Glu196Gln
ENST00000672818.3:c.577G>C	ENSP00000500891.1:p.Glu193Gln
ENST00000450313.6:c.512G>C	ENSP00000408176.2:p.Gly171Ala
ENST00000456914.7:c.502G>C MANE Select	ENSP00000407590.2:p.Glu168Gln
ENST00000461495.6:c.*241G>C	ENSP00000437166.1:n.*241G>C
ENST00000671856.1:n.448G>C
ENST00000671898.1:c.1090G>C	ENSP00000499896.1:p.Glu364Gln
ENST00000672011.1:c.470G>C	ENSP00000500418.1:p.Gly157Ala
ENST00000672314.1:c.502G>C	ENSP00000500828.1:p.Glu168Gln
ENST00000672593.1:c.*390G>C	ENSP00000500455.1:n.*390G>C
ENST00000672764.1:c.461G>C	ENSP00000500886.1:p.Gly154Ala
ENST00000672818.2:c.577G>C	ENSP00000500891.1:p.Glu193Gln
ENST00000673134.1:c.*199G>C	ENSP00000500526.1:n.*199G>C
ENST00000674679.1:c.530G>C	ENSP00000501623.1:n.530G>C
ENST00000354383.10:c.505G>C	ENSP00000346354.6:p.Glu169Gln
ENST00000355498.6:c.502G>C	ENSP00000347685.2:p.Glu168Gln
ENST00000372098.7:c.577G>C	ENSP00000361170.3:p.Glu193Gln
ENST00000372104.5:c.502G>C	ENSP00000361176.1:p.Glu168Gln
ENST00000372110.7:c.547G>C	ENSP00000361182.3:p.Glu183Gln
ENST00000372115.7:c.544G>C	ENSP00000361187.3:p.Glu182Gln
ENST00000412971.5:c.118G>C	ENSP00000410263.1:p.Glu40Gln
ENST00000435155.1:c.535G>C	ENSP00000403655.1:p.Glu179Gln
ENST00000448481.5:c.535G>C	ENSP00000409718.1:p.Glu179Gln
ENST00000450313.5:c.586G>C	ENSP00000408176.1:p.Glu196Gln
ENST00000456914.6:c.502G>C	ENSP00000407590.2:p.Glu168Gln
ENST00000461495.5:c.*241G>C	ENSP00000437166.1:n.*241G>C
ENST00000462388.5:n.193G>C
ENST00000467940.5:c.*425G>C	ENSP00000436478.1:n.*425G>C
ENST00000470256.5:c.389G>C	ENSP00000434985.1:p.Gly130Ala
ENST00000475516.5:c.*315G>C	ENSP00000433843.1:n.*315G>C
ENST00000478796.5:n.489G>C
ENST00000479746.6:n.860G>C
ENST00000481139.5:n.1050G>C
ENST00000481571.5:c.*315G>C	ENSP00000436597.1:n.*315G>C
ENST00000483642.5:n.1017G>C
ENST00000488731.6:c.187+85G>C	ENSP00000432330.1:n.187+85G>C
ENST00000492494.5:n.899G>C
ENST00000525160.5:c.*153G>C	ENSP00000431568.1:n.*153G>C
ENST00000528013.6:c.544G>C	ENSP00000433130.2:p.Glu182Gln
ENST00000529984.5:c.187+85G>C	ENSP00000437093.1:n.187+85G>C
ENST00000531105.5:c.115+1713G>C	ENSP00000431292.1:n.115+1713G>C
ENST00000533178.5:c.131G>C	ENSP00000436430.1:p.Gly44Ala
NM_001048171.1:c.544G>C	NP_001041636.1:p.Glu182Gln
NM_001048172.1:c.505G>C	NP_001041637.1:p.Glu169Gln
NM_001048173.1:c.502G>C	NP_001041638.1:p.Glu168Gln
NM_001048174.1:c.502G>C	NP_001041639.1:p.Glu168Gln
NM_001128425.1:c.586G>C , LRG_220t1:c.586G>C	NP_001121897.1:p.Glu196Gln
NM_001293190.1:c.547G>C	NP_001280119.1:p.Glu183Gln
NM_001293191.1:c.535G>C	NP_001280120.1:p.Glu179Gln
NM_001293192.1:c.226G>C	NP_001280121.1:p.Glu76Gln
NM_001293195.1:c.502G>C	NP_001280124.1:p.Glu168Gln
NM_001293196.1:c.226G>C	NP_001280125.1:p.Glu76Gln
NM_012222.2:c.577G>C	NP_036354.1:p.Glu193Gln
XM_011541497.1:c.562G>C	XP_011539799.1:p.Glu188Gln
XM_011541498.1:c.544G>C	XP_011539800.1:p.Glu182Gln
XM_011541499.1:c.544G>C	XP_011539801.1:p.Glu182Gln
XM_011541500.1:c.544G>C	XP_011539802.1:p.Glu182Gln
XM_011541501.1:c.544G>C	XP_011539803.1:p.Glu182Gln
XM_011541502.1:c.544G>C	XP_011539804.1:p.Glu182Gln
XM_011541503.1:c.544G>C	XP_011539805.1:p.Glu182Gln
XM_011541504.1:c.535G>C	XP_011539806.1:p.Glu179Gln
XM_011541505.1:c.124G>C	XP_011539807.1:p.Glu42Gln
XM_011541506.1:c.124G>C	XP_011539808.1:p.Glu42Gln
XM_011541507.1:c.115G>C	XP_011539809.1:p.Glu39Gln
XM_011541508.1:c.130G>C	XP_011539810.1:p.Glu44Gln
XR_946658.1:n.633G>C
NM_001350650.1:c.157G>C	NP_001337579.1:p.Glu53Gln
NM_001350651.1:c.157G>C	NP_001337580.1:p.Glu53Gln
NR_146882.1:n.760G>C
NR_146883.1:n.574G>C
XM_011541497.3:c.562G>C	XP_011539799.1:p.Glu188Gln
XM_011541500.3:c.544G>C	XP_011539802.1:p.Glu182Gln
XM_011541501.2:c.544G>C	XP_011539803.1:p.Glu182Gln
XM_011541502.2:c.544G>C	XP_011539804.1:p.Glu182Gln
XM_011541503.2:c.544G>C	XP_011539805.1:p.Glu182Gln
XM_011541504.2:c.535G>C	XP_011539806.1:p.Glu179Gln
XM_011541505.2:c.124G>C	XP_011539807.1:p.Glu42Gln
XM_011541506.2:c.124G>C	XP_011539808.1:p.Glu42Gln
XM_017001331.1:c.544G>C	XP_016856820.1:p.Glu182Gln
XM_017001332.1:c.544G>C	XP_016856821.1:p.Glu182Gln
XM_017001333.1:c.544G>C	XP_016856822.1:p.Glu182Gln
XM_017001334.1:c.505G>C	XP_016856823.1:p.Glu169Gln
XM_017001335.1:c.226G>C	XP_016856824.1:p.Glu76Gln
XM_017001336.1:c.157G>C	XP_016856825.1:p.Glu53Gln
XM_017001337.1:c.157G>C	XP_016856826.1:p.Glu53Gln
XM_024447244.1:c.157G>C	XP_024303012.1:p.Glu53Gln
XM_024447245.1:c.157G>C	XP_024303013.1:p.Glu53Gln
XM_024447248.1:c.115G>C	XP_024303016.1:p.Glu39Gln
XM_024447249.1:c.-15G>C	XP_024303017.1:n.-15G>C
XM_024447250.1:c.-15G>C	XP_024303018.1:n.-15G>C
XM_024447251.1:c.-15G>C	XP_024303019.1:n.-15G>C
XR_001737190.1:n.547G>C
XR_001737192.1:n.359G>C
XR_002956643.1:n.539G>C
XR_002956644.1:n.1074G>C
XR_946658.2:n.647G>C
NM_001048171.2:c.502G>C	NP_001041636.2:p.Glu168Gln
NM_001128425.2:c.586G>C MANE Plus Clinical	NP_001121897.1:p.Glu196Gln
NM_001048172.2:c.505G>C	NP_001041637.1:p.Glu169Gln
NM_001048173.2:c.502G>C	NP_001041638.1:p.Glu168Gln
NM_001048174.2:c.502G>C MANE Select	NP_001041639.1:p.Glu168Gln
NM_001293190.2:c.547G>C	NP_001280119.1:p.Glu183Gln
NM_001293191.2:c.535G>C	NP_001280120.1:p.Glu179Gln
NM_001293192.2:c.226G>C	NP_001280121.1:p.Glu76Gln
NM_001293195.2:c.502G>C	NP_001280124.1:p.Glu168Gln
NM_001293196.2:c.226G>C	NP_001280125.1:p.Glu76Gln
NM_001350650.2:c.157G>C	NP_001337579.1:p.Glu53Gln
NM_001350651.2:c.157G>C	NP_001337580.1:p.Glu53Gln
NM_012222.3:c.577G>C	NP_036354.1:p.Glu193Gln
NR_146882.2:n.730G>C
NR_146883.2:n.579G>C