Canonical Allele Identifier: CA1922577936

Gene: MAT1A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.80280305G= , CM000672.2:g.80280305G=	GRCh38
NC_000010.10:g.82040061G= , CM000672.1:g.82040061G=	GRCh37
NC_000010.9:g.82030041G=	NCBI36
NG_008083.1:g.14374C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372213.8:c.417C= MANE Select	ENSP00000361287.3:p.Phe139=
ENST00000372213.7:c.417C=	ENSP00000361287.3:p.Phe139=
ENST00000455001.1:c.228C=	ENSP00000414961.1:p.Phe76=
NM_000429.2:c.417C=	NP_000420.1:p.Phe139=
XM_005269842.3:c.417C=	XP_005269899.1:p.Phe139=
XM_005269843.3:c.294C=	XP_005269900.1:p.Phe98=
NM_000429.3:c.417C= MANE Select	NP_000420.1:p.Phe139=