Canonical Allele Identifier: CA1922573277
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275032C= , CM000672.2:g.80275032C= GRCh38
NC_000010.10:g.82034788C= , CM000672.1:g.82034788C= GRCh37
NC_000010.9:g.82024768C= NCBI36
NG_008083.1:g.19647G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.936G= MANE Select ENSP00000361287.3:p.Arg312=
ENST00000372213.7:c.936G= ENSP00000361287.3:p.Arg312=
ENST00000480845.1:n.168G=
ENST00000485270.5:n.448G=
NM_000429.2:c.936G= NP_000420.1:p.Arg312=
XM_005269842.3:c.936G= XP_005269899.1:p.Arg312=
XM_005269843.3:c.813G= XP_005269900.1:p.Arg271=
NM_000429.3:c.936G= MANE Select NP_000420.1:p.Arg312=