Canonical Allele Identifier: CA377360965
Gene: MAT1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275193C>A , CM000672.2:g.80275193C>A GRCh38
NC_000010.10:g.82034949C>A , CM000672.1:g.82034949C>A GRCh37
NC_000010.9:g.82024929C>A NCBI36
NG_008083.1:g.19486G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.775G>T MANE Select ENSP00000361287.3:p.Ala259Ser
ENST00000372213.7:c.775G>T ENSP00000361287.3:p.Ala259Ser
ENST00000480845.1:n.7G>T
ENST00000485270.5:n.287G>T
NM_000429.2:c.775G>T NP_000420.1:p.Ala259Ser
XM_005269842.3:c.775G>T XP_005269899.1:p.Ala259Ser
XM_005269843.3:c.652G>T XP_005269900.1:p.Ala218Ser
NM_000429.3:c.775G>T MANE Select NP_000420.1:p.Ala259Ser