Canonical Allele Identifier: CA417702231

Gene: MUTYH

Linked Data

• MyVariant Identifiers: chr1:g.45800070G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45334398G>C , CM000663.2:g.45334398G>C	GRCh38
NC_000001.10:g.45800070G>C , CM000663.1:g.45800070G>C	GRCh37
NC_000001.9:g.45572657G>C	NCBI36
NG_008189.1:g.11073C>G , LRG_220:g.11073C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000412971.6:c.37-1564C>G	ENSP00000410263.2:n.37-1564C>G
ENST00000435155.2:c.108C>G	ENSP00000403655.2:p.Ala36=
ENST00000467459.6:c.108C>G	ENSP00000435889.2:p.Ala36=
ENST00000483127.2:c.126C>G	ENSP00000436469.2:p.Ala42=
ENST00000485271.6:c.108C>G	ENSP00000431264.2:p.Ala36=
ENST00000529892.6:c.150C>G	ENSP00000432528.2:p.Ala50=
ENST00000533178.6:c.108C>G	ENSP00000436430.2:p.Ala36=
ENST00000672314.2:c.108C>G	ENSP00000500828.2:p.Ala36=
ENST00000674679.2:c.108C>G	ENSP00000501623.2:p.Ala36=
ENST00000710952.2:c.150C>G MANE Plus Clinical	ENSP00000518552.2:p.Ala50=
ENST00000672818.3:c.150C>G	ENSP00000500891.1:p.Ala50=
ENST00000450313.6:c.150C>G	ENSP00000408176.2:p.Ala50=
ENST00000456914.7:c.108C>G MANE Select	ENSP00000407590.2:p.Ala36=
ENST00000461495.6:c.150C>G	ENSP00000437166.1:p.Ala50=
ENST00000671856.1:n.128C>G
ENST00000671898.1:c.654C>G	ENSP00000499896.1:p.Ala218=
ENST00000672011.1:c.150C>G	ENSP00000500418.1:p.Ala50=
ENST00000672314.1:c.108C>G	ENSP00000500828.1:p.Ala36=
ENST00000672593.1:c.108C>G	ENSP00000500455.1:p.Ala36=
ENST00000672764.1:c.108C>G	ENSP00000500886.1:p.Ala36=
ENST00000672818.2:c.150C>G	ENSP00000500891.1:p.Ala50=
ENST00000673134.1:c.108C>G	ENSP00000500526.1:p.Ala36=
ENST00000674679.1:c.80C>G	ENSP00000501623.1:p.Pro27Arg
ENST00000354383.10:c.108C>G	ENSP00000346354.6:p.Ala36=
ENST00000355498.6:c.108C>G	ENSP00000347685.2:p.Ala36=
ENST00000372098.7:c.150C>G	ENSP00000361170.3:p.Ala50=
ENST00000372104.5:c.108C>G	ENSP00000361176.1:p.Ala36=
ENST00000372110.7:c.150C>G	ENSP00000361182.3:p.Ala50=
ENST00000372115.7:c.150C>G	ENSP00000361187.3:p.Ala50=
ENST00000412971.5:c.37-1564C>G	ENSP00000410263.1:n.37-1564C>G
ENST00000435155.1:c.108C>G	ENSP00000403655.1:p.Ala36=
ENST00000448481.5:c.108C>G	ENSP00000409718.1:p.Ala36=
ENST00000450313.5:c.150C>G	ENSP00000408176.1:p.Ala50=
ENST00000456914.6:c.108C>G	ENSP00000407590.2:p.Ala36=
ENST00000461495.5:c.150C>G	ENSP00000437166.1:p.Ala50=
ENST00000462387.5:n.328C>G
ENST00000467940.5:c.*28C>G	ENSP00000436478.1:n.*28C>G
ENST00000470256.5:c.108C>G	ENSP00000434985.1:p.Ala36=
ENST00000474703.1:n.230C>G
ENST00000475516.5:c.108C>G	ENSP00000433843.1:p.Ala36=
ENST00000476789.5:n.328C>G
ENST00000479746.6:n.171C>G
ENST00000481139.5:n.311C>G
ENST00000481571.5:c.150C>G	ENSP00000436597.1:p.Ala50=
ENST00000483127.1:c.126C>G	ENSP00000436469.1:p.Ala42=
ENST00000483642.5:n.289C>G
ENST00000485484.5:n.158C>G
ENST00000488731.6:c.108C>G	ENSP00000432330.1:p.Ala36=
ENST00000492494.5:n.171C>G
ENST00000525160.5:c.150C>G	ENSP00000431568.1:p.Ala50=
ENST00000528013.6:c.108C>G	ENSP00000433130.2:p.Ala36=
ENST00000529984.5:c.108C>G	ENSP00000437093.1:p.Ala36=
ENST00000531105.5:c.108C>G	ENSP00000431292.1:p.Ala36=
ENST00000533178.5:c.114C>G	ENSP00000436430.1:p.Ala38=
ENST00000534453.1:n.374C>G
NM_001048171.1:c.150C>G	NP_001041636.1:p.Ala50=
NM_001048172.1:c.108C>G	NP_001041637.1:p.Ala36=
NM_001048173.1:c.108C>G	NP_001041638.1:p.Ala36=
NM_001048174.1:c.108C>G	NP_001041639.1:p.Ala36=
NM_001128425.1:c.150C>G , LRG_220t1:c.150C>G	NP_001121897.1:p.Ala50=
NM_001293190.1:c.150C>G	NP_001280119.1:p.Ala50=
NM_001293191.1:c.108C>G	NP_001280120.1:p.Ala36=
NM_001293192.1:c.-105C>G	NP_001280121.1:n.-105C>G
NM_001293195.1:c.108C>G	NP_001280124.1:p.Ala36=
NM_001293196.1:c.-105C>G	NP_001280125.1:n.-105C>G
NM_012222.2:c.150C>G	NP_036354.1:p.Ala50=
XM_011541497.1:c.126C>G	XP_011539799.1:p.Ala42=
XM_011541498.1:c.108C>G	XP_011539800.1:p.Ala36=
XM_011541499.1:c.108C>G	XP_011539801.1:p.Ala36=
XM_011541500.1:c.108C>G	XP_011539802.1:p.Ala36=
XM_011541501.1:c.108C>G	XP_011539803.1:p.Ala36=
XM_011541502.1:c.108C>G	XP_011539804.1:p.Ala36=
XM_011541503.1:c.150C>G	XP_011539805.1:p.Ala50=
XM_011541504.1:c.108C>G	XP_011539806.1:p.Ala36=
XM_011541505.1:c.35C>G	XP_011539807.1:p.Pro12Arg
XM_011541506.1:c.35C>G	XP_011539808.1:p.Pro12Arg
XR_946658.1:n.197C>G
NM_001350650.1:c.-164C>G	NP_001337579.1:n.-164C>G
NM_001350651.1:c.-100C>G	NP_001337580.1:n.-100C>G
NR_146882.1:n.366C>G
NR_146883.1:n.254C>G
XM_011541497.3:c.126C>G	XP_011539799.1:p.Ala42=
XM_011541500.3:c.108C>G	XP_011539802.1:p.Ala36=
XM_011541501.2:c.108C>G	XP_011539803.1:p.Ala36=
XM_011541502.2:c.108C>G	XP_011539804.1:p.Ala36=
XM_011541503.2:c.150C>G	XP_011539805.1:p.Ala50=
XM_011541504.2:c.108C>G	XP_011539806.1:p.Ala36=
XM_011541505.2:c.35C>G	XP_011539807.1:p.Pro12Arg
XM_011541506.2:c.35C>G	XP_011539808.1:p.Pro12Arg
XM_017001331.1:c.108C>G	XP_016856820.1:p.Ala36=
XM_017001332.1:c.108C>G	XP_016856821.1:p.Ala36=
XM_017001333.1:c.108C>G	XP_016856822.1:p.Ala36=
XM_017001334.1:c.108C>G	XP_016856823.1:p.Ala36=
XM_017001335.1:c.-105C>G	XP_016856824.1:n.-105C>G
XM_017001336.1:c.-197C>G	XP_016856825.1:n.-197C>G
XM_017001337.1:c.-197C>G	XP_016856826.1:n.-197C>G
XM_024447244.1:c.-206C>G	XP_024303012.1:n.-206C>G
XM_024447245.1:c.-167C>G	XP_024303013.1:n.-167C>G
XM_024447248.1:c.-164C>G	XP_024303016.1:n.-164C>G
XM_024447249.1:c.-660C>G	XP_024303017.1:n.-660C>G
XM_024447250.1:c.-663C>G	XP_024303018.1:n.-663C>G
XM_024447251.1:c.-354C>G	XP_024303019.1:n.-354C>G
XR_001737190.1:n.217C>G
XR_001737192.1:n.145C>G
XR_002956643.1:n.325C>G
XR_002956644.1:n.343C>G
XR_946658.2:n.211C>G
NM_001048171.2:c.108C>G	NP_001041636.2:p.Ala36=
NM_001128425.2:c.150C>G MANE Plus Clinical	NP_001121897.1:p.Ala50=
NM_001048172.2:c.108C>G	NP_001041637.1:p.Ala36=
NM_001048173.2:c.108C>G	NP_001041638.1:p.Ala36=
NM_001048174.2:c.108C>G MANE Select	NP_001041639.1:p.Ala36=
NM_001293190.2:c.150C>G	NP_001280119.1:p.Ala50=
NM_001293191.2:c.108C>G	NP_001280120.1:p.Ala36=
NM_001293192.2:c.-105C>G	NP_001280121.1:n.-105C>G
NM_001293195.2:c.108C>G	NP_001280124.1:p.Ala36=
NM_001293196.2:c.-105C>G	NP_001280125.1:n.-105C>G
NM_001350650.2:c.-164C>G	NP_001337579.1:n.-164C>G
NM_001350651.2:c.-100C>G	NP_001337580.1:n.-100C>G
NM_012222.3:c.150C>G	NP_036354.1:p.Ala50=
NR_146882.2:n.336C>G
NR_146883.2:n.259C>G