Canonical Allele Identifier: CA417702269

Gene: MUTYH

Linked Data

• dbSNP Id: rs1570465862
• MyVariant Identifiers: chr1:g.45800145A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45334473A>T , CM000663.2:g.45334473A>T	GRCh38
NC_000001.10:g.45800145A>T , CM000663.1:g.45800145A>T	GRCh37
NC_000001.9:g.45572732A>T	NCBI36
NG_008189.1:g.10998T>A , LRG_220:g.10998T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412971.6:c.37-1639T>A	ENSP00000410263.2:n.37-1639T>A
ENST00000435155.2:c.33T>A	ENSP00000403655.2:p.Gly11=
ENST00000467459.6:c.33T>A	ENSP00000435889.2:p.Gly11=
ENST00000483127.2:c.51T>A	ENSP00000436469.2:p.Gly17=
ENST00000485271.6:c.33T>A	ENSP00000431264.2:p.Gly11=
ENST00000529892.6:c.75T>A	ENSP00000432528.2:p.Gly25=
ENST00000533178.6:c.33T>A	ENSP00000436430.2:p.Gly11=
ENST00000672314.2:c.33T>A	ENSP00000500828.2:p.Gly11=
ENST00000674679.2:c.33T>A	ENSP00000501623.2:p.Gly11=
ENST00000710952.2:c.75T>A MANE Plus Clinical	ENSP00000518552.2:p.Gly25=
ENST00000672818.3:c.75T>A	ENSP00000500891.1:p.Gly25=
ENST00000450313.6:c.75T>A	ENSP00000408176.2:p.Gly25=
ENST00000456914.7:c.33T>A MANE Select	ENSP00000407590.2:p.Gly11=
ENST00000461495.6:c.75T>A	ENSP00000437166.1:p.Gly25=
ENST00000671856.1:n.53T>A
ENST00000671898.1:c.579T>A	ENSP00000499896.1:p.Gly193=
ENST00000672011.1:c.75T>A	ENSP00000500418.1:p.Gly25=
ENST00000672314.1:c.33T>A	ENSP00000500828.1:p.Gly11=
ENST00000672593.1:c.33T>A	ENSP00000500455.1:p.Gly11=
ENST00000672764.1:c.33T>A	ENSP00000500886.1:p.Gly11=
ENST00000672818.2:c.75T>A	ENSP00000500891.1:p.Gly25=
ENST00000673134.1:c.33T>A	ENSP00000500526.1:p.Gly11=
ENST00000674679.1:c.5T>A	ENSP00000501623.1:p.Val2Asp
ENST00000354383.10:c.33T>A	ENSP00000346354.6:p.Gly11=
ENST00000355498.6:c.33T>A	ENSP00000347685.2:p.Gly11=
ENST00000372098.7:c.75T>A	ENSP00000361170.3:p.Gly25=
ENST00000372104.5:c.33T>A	ENSP00000361176.1:p.Gly11=
ENST00000372110.7:c.75T>A	ENSP00000361182.3:p.Gly25=
ENST00000372115.7:c.75T>A	ENSP00000361187.3:p.Gly25=
ENST00000412971.5:c.37-1639T>A	ENSP00000410263.1:n.37-1639T>A
ENST00000435155.1:c.33T>A	ENSP00000403655.1:p.Gly11=
ENST00000448481.5:c.33T>A	ENSP00000409718.1:p.Gly11=
ENST00000450313.5:c.75T>A	ENSP00000408176.1:p.Gly25=
ENST00000456914.6:c.33T>A	ENSP00000407590.2:p.Gly11=
ENST00000461495.5:c.75T>A	ENSP00000437166.1:p.Gly25=
ENST00000462387.5:n.253T>A
ENST00000467940.5:c.91T>A	ENSP00000436478.1:p.Ser31Thr
ENST00000470256.5:c.33T>A	ENSP00000434985.1:p.Gly11=
ENST00000474703.1:n.155T>A
ENST00000475516.5:c.33T>A	ENSP00000433843.1:p.Gly11=
ENST00000476789.5:n.253T>A
ENST00000479746.6:n.96T>A
ENST00000481139.5:n.236T>A
ENST00000481571.5:c.75T>A	ENSP00000436597.1:p.Gly25=
ENST00000483127.1:c.51T>A	ENSP00000436469.1:p.Gly17=
ENST00000483642.5:n.214T>A
ENST00000485484.5:n.83T>A
ENST00000488731.6:c.33T>A	ENSP00000432330.1:p.Gly11=
ENST00000492494.5:n.96T>A
ENST00000525160.5:c.75T>A	ENSP00000431568.1:p.Gly25=
ENST00000528013.6:c.33T>A	ENSP00000433130.2:p.Gly11=
ENST00000529984.5:c.33T>A	ENSP00000437093.1:p.Gly11=
ENST00000531105.5:c.33T>A	ENSP00000431292.1:p.Gly11=
ENST00000533178.5:c.39T>A	ENSP00000436430.1:p.Gly13=
ENST00000534453.1:n.299T>A
NM_001048171.1:c.75T>A	NP_001041636.1:p.Gly25=
NM_001048172.1:c.33T>A	NP_001041637.1:p.Gly11=
NM_001048173.1:c.33T>A	NP_001041638.1:p.Gly11=
NM_001048174.1:c.33T>A	NP_001041639.1:p.Gly11=
NM_001128425.1:c.75T>A , LRG_220t1:c.75T>A	NP_001121897.1:p.Gly25=
NM_001293190.1:c.75T>A	NP_001280119.1:p.Gly25=
NM_001293191.1:c.33T>A	NP_001280120.1:p.Gly11=
NM_001293192.1:c.-180T>A	NP_001280121.1:n.-180T>A
NM_001293195.1:c.33T>A	NP_001280124.1:p.Gly11=
NM_001293196.1:c.-180T>A	NP_001280125.1:n.-180T>A
NM_012222.2:c.75T>A	NP_036354.1:p.Gly25=
XM_011541497.1:c.51T>A	XP_011539799.1:p.Gly17=
XM_011541498.1:c.33T>A	XP_011539800.1:p.Gly11=
XM_011541499.1:c.33T>A	XP_011539801.1:p.Gly11=
XM_011541500.1:c.33T>A	XP_011539802.1:p.Gly11=
XM_011541501.1:c.33T>A	XP_011539803.1:p.Gly11=
XM_011541502.1:c.33T>A	XP_011539804.1:p.Gly11=
XM_011541503.1:c.75T>A	XP_011539805.1:p.Gly25=
XM_011541504.1:c.33T>A	XP_011539806.1:p.Gly11=
XM_011541505.1:c.-41T>A	XP_011539807.1:n.-41T>A
XM_011541506.1:c.-41T>A	XP_011539808.1:n.-41T>A
XR_946658.1:n.122T>A
NM_001350650.1:c.-239T>A	NP_001337579.1:n.-239T>A
NM_001350651.1:c.-175T>A	NP_001337580.1:n.-175T>A
NR_146882.1:n.291T>A
NR_146883.1:n.179T>A
XM_011541497.3:c.51T>A	XP_011539799.1:p.Gly17=
XM_011541500.3:c.33T>A	XP_011539802.1:p.Gly11=
XM_011541501.2:c.33T>A	XP_011539803.1:p.Gly11=
XM_011541502.2:c.33T>A	XP_011539804.1:p.Gly11=
XM_011541503.2:c.75T>A	XP_011539805.1:p.Gly25=
XM_011541504.2:c.33T>A	XP_011539806.1:p.Gly11=
XM_011541505.2:c.-41T>A	XP_011539807.1:n.-41T>A
XM_011541506.2:c.-41T>A	XP_011539808.1:n.-41T>A
XM_017001331.1:c.33T>A	XP_016856820.1:p.Gly11=
XM_017001332.1:c.33T>A	XP_016856821.1:p.Gly11=
XM_017001333.1:c.33T>A	XP_016856822.1:p.Gly11=
XM_017001334.1:c.33T>A	XP_016856823.1:p.Gly11=
XM_017001335.1:c.-180T>A	XP_016856824.1:n.-180T>A
XM_017001336.1:c.-272T>A	XP_016856825.1:n.-272T>A
XM_017001337.1:c.-272T>A	XP_016856826.1:n.-272T>A
XM_024447244.1:c.-281T>A	XP_024303012.1:n.-281T>A
XM_024447245.1:c.-242T>A	XP_024303013.1:n.-242T>A
XM_024447248.1:c.-239T>A	XP_024303016.1:n.-239T>A
XM_024447249.1:c.-735T>A	XP_024303017.1:n.-735T>A
XM_024447250.1:c.-738T>A	XP_024303018.1:n.-738T>A
XM_024447251.1:c.-429T>A	XP_024303019.1:n.-429T>A
XR_001737190.1:n.142T>A
XR_001737192.1:n.70T>A
XR_002956643.1:n.250T>A
XR_002956644.1:n.268T>A
XR_946658.2:n.136T>A
NM_001048171.2:c.33T>A	NP_001041636.2:p.Gly11=
NM_001128425.2:c.75T>A MANE Plus Clinical	NP_001121897.1:p.Gly25=
NM_001048172.2:c.33T>A	NP_001041637.1:p.Gly11=
NM_001048173.2:c.33T>A	NP_001041638.1:p.Gly11=
NM_001048174.2:c.33T>A MANE Select	NP_001041639.1:p.Gly11=
NM_001293190.2:c.75T>A	NP_001280119.1:p.Gly25=
NM_001293191.2:c.33T>A	NP_001280120.1:p.Gly11=
NM_001293192.2:c.-180T>A	NP_001280121.1:n.-180T>A
NM_001293195.2:c.33T>A	NP_001280124.1:p.Gly11=
NM_001293196.2:c.-180T>A	NP_001280125.1:n.-180T>A
NM_001350650.2:c.-239T>A	NP_001337579.1:n.-239T>A
NM_001350651.2:c.-175T>A	NP_001337580.1:n.-175T>A
NM_012222.3:c.75T>A	NP_036354.1:p.Gly25=
NR_146882.2:n.261T>A
NR_146883.2:n.184T>A