Canonical Allele Identifier: CA1922573212

Gene: MAT1A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.80274956G= , CM000672.2:g.80274956G=	GRCh38
NC_000010.10:g.82034712G= , CM000672.1:g.82034712G=	GRCh37
NC_000010.9:g.82024692G=	NCBI36
NG_008083.1:g.19723C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372213.8:c.951+61C= MANE Select	ENSP00000361287.3:n.951+61C=
ENST00000372213.7:c.951+61C=	ENSP00000361287.3:n.951+61C=
ENST00000480845.1:n.183+61C=
ENST00000485270.5:n.463+61C=
NM_000429.2:c.951+61C=	NP_000420.1:n.951+61C=
XM_005269842.3:c.951+61C=	XP_005269899.1:n.951+61C=
XM_005269843.3:c.828+61C=	XP_005269900.1:n.828+61C=
NM_000429.3:c.951+61C= MANE Select	NP_000420.1:n.951+61C=