Canonical Allele Identifier: CA417880241

Gene: MUTYH

Linked Data

• MyVariant Identifiers: chr1:g.45798107G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45332435G>C , CM000663.2:g.45332435G>C	GRCh38
NC_000001.10:g.45798107G>C , CM000663.1:g.45798107G>C	GRCh37
NC_000001.9:g.45570694G>C	NCBI36
NG_008189.1:g.13036C>G , LRG_220:g.13036C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412971.6:c.276C>G	ENSP00000410263.2:p.Ala92=
ENST00000435155.2:c.693C>G	ENSP00000403655.2:p.Ala231=
ENST00000467459.6:c.660C>G	ENSP00000435889.2:p.Ala220=
ENST00000483127.2:c.678C>G	ENSP00000436469.2:p.Ala226=
ENST00000485271.6:c.660C>G	ENSP00000431264.2:p.Ala220=
ENST00000529892.6:c.702C>G	ENSP00000432528.2:p.Ala234=
ENST00000533178.6:c.283C>G	ENSP00000436430.2:p.His95Asp
ENST00000672314.2:c.660C>G	ENSP00000500828.2:p.Ala220=
ENST00000674679.2:c.*572C>G	ENSP00000501623.2:n.*572C>G
ENST00000710952.2:c.744C>G MANE Plus Clinical	ENSP00000518552.2:p.Ala248=
ENST00000672818.3:c.735C>G	ENSP00000500891.1:p.Ala245=
ENST00000450313.6:c.670C>G	ENSP00000408176.2:p.His224Asp
ENST00000456914.7:c.660C>G MANE Select	ENSP00000407590.2:p.Ala220=
ENST00000461495.6:c.*399C>G	ENSP00000437166.1:n.*399C>G
ENST00000671898.1:c.1248C>G	ENSP00000499896.1:p.Ala416=
ENST00000672011.1:c.628C>G	ENSP00000500418.1:p.His210Asp
ENST00000672314.1:c.660C>G	ENSP00000500828.1:p.Ala220=
ENST00000672593.1:c.*633C>G	ENSP00000500455.1:n.*633C>G
ENST00000672764.1:c.619C>G	ENSP00000500886.1:p.His207Asp
ENST00000672818.2:c.735C>G	ENSP00000500891.1:p.Ala245=
ENST00000673134.1:c.*357C>G	ENSP00000500526.1:n.*357C>G
ENST00000674679.1:c.688C>G	ENSP00000501623.1:n.688C>G
ENST00000354383.10:c.663C>G	ENSP00000346354.6:p.Ala221=
ENST00000355498.6:c.660C>G	ENSP00000347685.2:p.Ala220=
ENST00000372098.7:c.735C>G	ENSP00000361170.3:p.Ala245=
ENST00000372104.5:c.660C>G	ENSP00000361176.1:p.Ala220=
ENST00000372110.7:c.705C>G	ENSP00000361182.3:p.Ala235=
ENST00000372115.7:c.702C>G	ENSP00000361187.3:p.Ala234=
ENST00000412971.5:c.276C>G	ENSP00000410263.1:p.Ala92=
ENST00000435155.1:c.693C>G	ENSP00000403655.1:p.Ala231=
ENST00000448481.5:c.693C>G	ENSP00000409718.1:p.Ala231=
ENST00000450313.5:c.744C>G	ENSP00000408176.1:p.Ala248=
ENST00000456914.6:c.660C>G	ENSP00000407590.2:p.Ala220=
ENST00000461495.5:c.*399C>G	ENSP00000437166.1:n.*399C>G
ENST00000462388.5:n.351C>G
ENST00000467459.5:c.54C>G	ENSP00000435889.1:p.Ala18=
ENST00000467940.5:c.*583C>G	ENSP00000436478.1:n.*583C>G
ENST00000470256.5:c.547C>G	ENSP00000434985.1:p.His183Asp
ENST00000475516.5:c.*473C>G	ENSP00000433843.1:n.*473C>G
ENST00000478796.5:n.647C>G
ENST00000481571.5:c.*473C>G	ENSP00000436597.1:n.*473C>G
ENST00000488731.6:c.187+328C>G	ENSP00000432330.1:n.187+328C>G
ENST00000525160.5:c.*311C>G	ENSP00000431568.1:n.*311C>G
ENST00000528013.6:c.702C>G	ENSP00000433130.2:p.Ala234=
ENST00000529984.5:c.187+328C>G	ENSP00000437093.1:n.187+328C>G
ENST00000531105.5:c.115+1956C>G	ENSP00000431292.1:n.115+1956C>G
ENST00000533178.5:c.289C>G	ENSP00000436430.1:p.His97Asp
NM_001048171.1:c.702C>G	NP_001041636.1:p.Ala234=
NM_001048172.1:c.663C>G	NP_001041637.1:p.Ala221=
NM_001048173.1:c.660C>G	NP_001041638.1:p.Ala220=
NM_001048174.1:c.660C>G	NP_001041639.1:p.Ala220=
NM_001128425.1:c.744C>G , LRG_220t1:c.744C>G	NP_001121897.1:p.Ala248=
NM_001293190.1:c.705C>G	NP_001280119.1:p.Ala235=
NM_001293191.1:c.693C>G	NP_001280120.1:p.Ala231=
NM_001293192.1:c.384C>G	NP_001280121.1:p.Ala128=
NM_001293195.1:c.660C>G	NP_001280124.1:p.Ala220=
NM_001293196.1:c.384C>G	NP_001280125.1:p.Ala128=
NM_012222.2:c.735C>G	NP_036354.1:p.Ala245=
XM_011541497.1:c.720C>G	XP_011539799.1:p.Ala240=
XM_011541498.1:c.702C>G	XP_011539800.1:p.Ala234=
XM_011541499.1:c.702C>G	XP_011539801.1:p.Ala234=
XM_011541500.1:c.702C>G	XP_011539802.1:p.Ala234=
XM_011541501.1:c.702C>G	XP_011539803.1:p.Ala234=
XM_011541502.1:c.702C>G	XP_011539804.1:p.Ala234=
XM_011541503.1:c.702C>G	XP_011539805.1:p.Ala234=
XM_011541504.1:c.693C>G	XP_011539806.1:p.Ala231=
XM_011541505.1:c.282C>G	XP_011539807.1:p.Ala94=
XM_011541506.1:c.282C>G	XP_011539808.1:p.Ala94=
XM_011541507.1:c.273C>G	XP_011539809.1:p.Ala91=
XM_011541508.1:c.288C>G	XP_011539810.1:p.Ala96=
XR_946658.1:n.791C>G
NM_001350650.1:c.315C>G	NP_001337579.1:p.Ala105=
NM_001350651.1:c.315C>G	NP_001337580.1:p.Ala105=
NR_146882.1:n.918C>G
NR_146883.1:n.732C>G
XM_011541497.3:c.720C>G	XP_011539799.1:p.Ala240=
XM_011541500.3:c.702C>G	XP_011539802.1:p.Ala234=
XM_011541501.2:c.702C>G	XP_011539803.1:p.Ala234=
XM_011541502.2:c.702C>G	XP_011539804.1:p.Ala234=
XM_011541503.2:c.702C>G	XP_011539805.1:p.Ala234=
XM_011541504.2:c.693C>G	XP_011539806.1:p.Ala231=
XM_011541505.2:c.282C>G	XP_011539807.1:p.Ala94=
XM_011541506.2:c.282C>G	XP_011539808.1:p.Ala94=
XM_017001331.1:c.702C>G	XP_016856820.1:p.Ala234=
XM_017001332.1:c.702C>G	XP_016856821.1:p.Ala234=
XM_017001333.1:c.702C>G	XP_016856822.1:p.Ala234=
XM_017001334.1:c.663C>G	XP_016856823.1:p.Ala221=
XM_017001335.1:c.384C>G	XP_016856824.1:p.Ala128=
XM_017001336.1:c.315C>G	XP_016856825.1:p.Ala105=
XM_017001337.1:c.315C>G	XP_016856826.1:p.Ala105=
XM_024447244.1:c.315C>G	XP_024303012.1:p.Ala105=
XM_024447245.1:c.315C>G	XP_024303013.1:p.Ala105=
XM_024447248.1:c.273C>G	XP_024303016.1:p.Ala91=
XM_024447249.1:c.144C>G	XP_024303017.1:p.Ala48=
XM_024447250.1:c.144C>G	XP_024303018.1:p.Ala48=
XM_024447251.1:c.144C>G	XP_024303019.1:p.Ala48=
XR_001737190.1:n.705C>G
XR_001737192.1:n.517C>G
XR_002956643.1:n.697C>G
XR_002956644.1:n.1232C>G
XR_946658.2:n.805C>G
NM_001048171.2:c.660C>G	NP_001041636.2:p.Ala220=
NM_001128425.2:c.744C>G MANE Plus Clinical	NP_001121897.1:p.Ala248=
NM_001048172.2:c.663C>G	NP_001041637.1:p.Ala221=
NM_001048173.2:c.660C>G	NP_001041638.1:p.Ala220=
NM_001048174.2:c.660C>G MANE Select	NP_001041639.1:p.Ala220=
NM_001293190.2:c.705C>G	NP_001280119.1:p.Ala235=
NM_001293191.2:c.693C>G	NP_001280120.1:p.Ala231=
NM_001293192.2:c.384C>G	NP_001280121.1:p.Ala128=
NM_001293195.2:c.660C>G	NP_001280124.1:p.Ala220=
NM_001293196.2:c.384C>G	NP_001280125.1:p.Ala128=
NM_001350650.2:c.315C>G	NP_001337579.1:p.Ala105=
NM_001350651.2:c.315C>G	NP_001337580.1:p.Ala105=
NM_012222.3:c.735C>G	NP_036354.1:p.Ala245=
NR_146882.2:n.888C>G
NR_146883.2:n.737C>G