Canonical Allele Identifier: CA377362675

Gene: MAT1A

Linked Data

• MyVariant Identifiers: chr10:g.82039974C>A (hg19) ; chr10:g.80280218C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.80280218C>A , CM000672.2:g.80280218C>A	GRCh38
NC_000010.10:g.82039974C>A , CM000672.1:g.82039974C>A	GRCh37
NC_000010.9:g.82029954C>A	NCBI36
NG_008083.1:g.14461G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372213.8:c.504G>T MANE Select	ENSP00000361287.3:p.Arg168Ser
ENST00000372213.7:c.504G>T	ENSP00000361287.3:p.Arg168Ser
ENST00000455001.1:c.315G>T	ENSP00000414961.1:p.Arg105Ser
NM_000429.2:c.504G>T	NP_000420.1:p.Arg168Ser
XM_005269842.3:c.504G>T	XP_005269899.1:p.Arg168Ser
XM_005269843.3:c.381G>T	XP_005269900.1:p.Arg127Ser
NM_000429.3:c.504G>T MANE Select	NP_000420.1:p.Arg168Ser