Canonical Allele Identifier: CA377360666
Gene: MAT1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275081T>A , CM000672.2:g.80275081T>A GRCh38
NC_000010.10:g.82034837T>A , CM000672.1:g.82034837T>A GRCh37
NC_000010.9:g.82024817T>A NCBI36
NG_008083.1:g.19598A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.887A>T MANE Select ENSP00000361287.3:p.Tyr296Phe
ENST00000372213.7:c.887A>T ENSP00000361287.3:p.Tyr296Phe
ENST00000480845.1:n.119A>T
ENST00000485270.5:n.399A>T
NM_000429.2:c.887A>T NP_000420.1:p.Tyr296Phe
XM_005269842.3:c.887A>T XP_005269899.1:p.Tyr296Phe
XM_005269843.3:c.764A>T XP_005269900.1:p.Tyr255Phe
NM_000429.3:c.887A>T MANE Select NP_000420.1:p.Tyr296Phe