Canonical Allele Identifier: CA470467322

Gene: MAT1A

Linked Data

• MyVariant Identifiers: chr10:g.82034800T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.80275044T>G , CM000672.2:g.80275044T>G	GRCh38
NC_000010.10:g.82034800T>G , CM000672.1:g.82034800T>G	GRCh37
NC_000010.9:g.82024780T>G	NCBI36
NG_008083.1:g.19635A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372213.8:c.924A>C MANE Select	ENSP00000361287.3:p.Ala308=
ENST00000372213.7:c.924A>C	ENSP00000361287.3:p.Ala308=
ENST00000480845.1:n.156A>C
ENST00000485270.5:n.436A>C
NM_000429.2:c.924A>C	NP_000420.1:p.Ala308=
XM_005269842.3:c.924A>C	XP_005269899.1:p.Ala308=
XM_005269843.3:c.801A>C	XP_005269900.1:p.Ala267=
NM_000429.3:c.924A>C MANE Select	NP_000420.1:p.Ala308=