Canonical Allele Identifier: CA1922573405
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275094G= , CM000672.2:g.80275094G= GRCh38
NC_000010.10:g.82034850G= , CM000672.1:g.82034850G= GRCh37
NC_000010.9:g.82024830G= NCBI36
NG_008083.1:g.19585C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.874C= MANE Select ENSP00000361287.3:p.Arg292=
ENST00000372213.7:c.874C= ENSP00000361287.3:p.Arg292=
ENST00000480845.1:n.106C=
ENST00000485270.5:n.386C=
NM_000429.2:c.874C= NP_000420.1:p.Arg292=
XM_005269842.3:c.874C= XP_005269899.1:p.Arg292=
XM_005269843.3:c.751C= XP_005269900.1:p.Arg251=
NM_000429.3:c.874C= MANE Select NP_000420.1:p.Arg292=