Canonical Allele Identifier: CA1922577852

Gene: MAT1A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.80280195A= , CM000672.2:g.80280195A=	GRCh38
NC_000010.10:g.82039951A= , CM000672.1:g.82039951A=	GRCh37
NC_000010.9:g.82029931A=	NCBI36
NG_008083.1:g.14484T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000372213.8:c.527T= MANE Select	ENSP00000361287.3:p.Leu176=
ENST00000372213.7:c.527T=	ENSP00000361287.3:p.Leu176=
ENST00000455001.1:c.338T=	ENSP00000414961.1:p.Leu113=
NM_000429.2:c.527T=	NP_000420.1:p.Leu176=
XM_005269842.3:c.527T=	XP_005269899.1:p.Leu176=
XM_005269843.3:c.404T=	XP_005269900.1:p.Leu135=
NM_000429.3:c.527T= MANE Select	NP_000420.1:p.Leu176=