Canonical Allele Identifier: CA377362757
Gene: MAT1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80280256G>A , CM000672.2:g.80280256G>A GRCh38
NC_000010.10:g.82040012G>A , CM000672.1:g.82040012G>A GRCh37
NC_000010.9:g.82029992G>A NCBI36
NG_008083.1:g.14423C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.466C>T MANE Select ENSP00000361287.3:p.Leu156Phe
ENST00000372213.7:c.466C>T ENSP00000361287.3:p.Leu156Phe
ENST00000455001.1:c.277C>T ENSP00000414961.1:p.Leu93Phe
NM_000429.2:c.466C>T NP_000420.1:p.Leu156Phe
XM_005269842.3:c.466C>T XP_005269899.1:p.Leu156Phe
XM_005269843.3:c.343C>T XP_005269900.1:p.Leu115Phe
NM_000429.3:c.466C>T MANE Select NP_000420.1:p.Leu156Phe