Canonical Allele Identifier: CA1922573442

Gene: MAT1A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.80275117C= , CM000672.2:g.80275117C=	GRCh38
NC_000010.10:g.82034873C= , CM000672.1:g.82034873C=	GRCh37
NC_000010.9:g.82024853C=	NCBI36
NG_008083.1:g.19562G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372213.8:c.851G= MANE Select	ENSP00000361287.3:p.Gly284=
ENST00000372213.7:c.851G=	ENSP00000361287.3:p.Gly284=
ENST00000480845.1:n.83G=
ENST00000485270.5:n.363G=
NM_000429.2:c.851G=	NP_000420.1:p.Gly284=
XM_005269842.3:c.851G=	XP_005269899.1:p.Gly284=
XM_005269843.3:c.728G=	XP_005269900.1:p.Gly243=
NM_000429.3:c.851G= MANE Select	NP_000420.1:p.Gly284=