Canonical Allele Identifier: CA1922573449

Gene: MAT1A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.80275125G= , CM000672.2:g.80275125G=	GRCh38
NC_000010.10:g.82034881G= , CM000672.1:g.82034881G=	GRCh37
NC_000010.9:g.82024861G=	NCBI36
NG_008083.1:g.19554C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372213.8:c.843C= MANE Select	ENSP00000361287.3:p.Ala281=
ENST00000372213.7:c.843C=	ENSP00000361287.3:p.Ala281=
ENST00000480845.1:n.75C=
ENST00000485270.5:n.355C=
NM_000429.2:c.843C=	NP_000420.1:p.Ala281=
XM_005269842.3:c.843C=	XP_005269899.1:p.Ala281=
XM_005269843.3:c.720C=	XP_005269900.1:p.Ala240=
NM_000429.3:c.843C= MANE Select	NP_000420.1:p.Ala281=