Canonical Allele Identifier: CA1922577927

Gene: MAT1A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.80280286T= , CM000672.2:g.80280286T=	GRCh38
NC_000010.10:g.82040042T= , CM000672.1:g.82040042T=	GRCh37
NC_000010.9:g.82030022T=	NCBI36
NG_008083.1:g.14393A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372213.8:c.436A= MANE Select	ENSP00000361287.3:p.Thr146=
ENST00000372213.7:c.436A=	ENSP00000361287.3:p.Thr146=
ENST00000455001.1:c.247A=	ENSP00000414961.1:p.Thr83=
NM_000429.2:c.436A=	NP_000420.1:p.Thr146=
XM_005269842.3:c.436A=	XP_005269899.1:p.Thr146=
XM_005269843.3:c.313A=	XP_005269900.1:p.Thr105=
NM_000429.3:c.436A= MANE Select	NP_000420.1:p.Thr146=