Canonical Allele Identifier: CA377360983
Gene: MAT1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275198C>A , CM000672.2:g.80275198C>A GRCh38
NC_000010.10:g.82034954C>A , CM000672.1:g.82034954C>A GRCh37
NC_000010.9:g.82024934C>A NCBI36
NG_008083.1:g.19481G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.770G>T MANE Select ENSP00000361287.3:p.Gly257Val
ENST00000372213.7:c.770G>T ENSP00000361287.3:p.Gly257Val
ENST00000480845.1:n.2G>T
ENST00000485270.5:n.282G>T
NM_000429.2:c.770G>T NP_000420.1:p.Gly257Val
XM_005269842.3:c.770G>T XP_005269899.1:p.Gly257Val
XM_005269843.3:c.647G>T XP_005269900.1:p.Gly216Val
NM_000429.3:c.770G>T MANE Select NP_000420.1:p.Gly257Val