Canonical Allele Identifier: CA1922577837
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80274521T= , CM000672.2:g.80274521T= GRCh38
NC_000010.10:g.82034277T= , CM000672.1:g.82034277T= GRCh37
NC_000010.9:g.82024257T= NCBI36
NG_008083.1:g.20158A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.1084A= MANE Select ENSP00000361287.3:p.Arg362=
ENST00000372213.7:c.1084A= ENSP00000361287.3:p.Arg362=
ENST00000480845.1:n.316A=
ENST00000485270.5:n.596A=
NM_000429.2:c.1084A= NP_000420.1:p.Arg362=
XM_005269842.3:c.1084A= XP_005269899.1:p.Arg362=
XM_005269843.3:c.961A= XP_005269900.1:p.Arg321=
NM_000429.3:c.1084A= MANE Select NP_000420.1:p.Arg362=