Canonical Allele Identifier: CA470467202

Gene: MAT1A

Linked Data

• MyVariant Identifiers: chr10:g.82033629A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.80273873A>G , CM000672.2:g.80273873A>G	GRCh38
NC_000010.10:g.82033629A>G , CM000672.1:g.82033629A>G	GRCh37
NC_000010.9:g.82023609A>G	NCBI36
NG_008083.1:g.20806T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372213.8:c.1096T>C MANE Select	ENSP00000361287.3:p.Leu366=
ENST00000372213.7:c.1096T>C	ENSP00000361287.3:p.Leu366=
ENST00000480845.1:n.328T>C
ENST00000485270.5:n.608T>C
NM_000429.2:c.1096T>C	NP_000420.1:p.Leu366=
XM_005269842.3:c.1096T>C	XP_005269899.1:p.Leu366=
XM_005269843.3:c.973T>C	XP_005269900.1:p.Leu325=
NM_000429.3:c.1096T>C MANE Select	NP_000420.1:p.Leu366=