Canonical Allele Identifier: CA377362897
Gene: MAT1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80280316C>T , CM000672.2:g.80280316C>T GRCh38
NC_000010.10:g.82040072C>T , CM000672.1:g.82040072C>T GRCh37
NC_000010.9:g.82030052C>T NCBI36
NG_008083.1:g.14363G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.406G>A MANE Select ENSP00000361287.3:p.Gly136Ser
ENST00000372213.7:c.406G>A ENSP00000361287.3:p.Gly136Ser
ENST00000455001.1:c.217G>A ENSP00000414961.1:p.Gly73Ser
NM_000429.2:c.406G>A NP_000420.1:p.Gly136Ser
XM_005269842.3:c.406G>A XP_005269899.1:p.Gly136Ser
XM_005269843.3:c.283G>A XP_005269900.1:p.Gly95Ser
NM_000429.3:c.406G>A MANE Select NP_000420.1:p.Gly136Ser