Canonical Allele Identifier: CA1922573604
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275197C= , CM000672.2:g.80275197C= GRCh38
NC_000010.10:g.82034953C= , CM000672.1:g.82034953C= GRCh37
NC_000010.9:g.82024933C= NCBI36
NG_008083.1:g.19482G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.771G= MANE Select ENSP00000361287.3:p.Gly257=
ENST00000372213.7:c.771G= ENSP00000361287.3:p.Gly257=
ENST00000480845.1:n.3G=
ENST00000485270.5:n.283G=
NM_000429.2:c.771G= NP_000420.1:p.Gly257=
XM_005269842.3:c.771G= XP_005269899.1:p.Gly257=
XM_005269843.3:c.648G= XP_005269900.1:p.Gly216=
NM_000429.3:c.771G= MANE Select NP_000420.1:p.Gly257=