Canonical Allele Identifier: CA1922573391
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275090G= , CM000672.2:g.80275090G= GRCh38
NC_000010.10:g.82034846G= , CM000672.1:g.82034846G= GRCh37
NC_000010.9:g.82024826G= NCBI36
NG_008083.1:g.19589C=

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.878C= MANE Select ENSP00000361287.3:p.Ser293=
ENST00000372213.7:c.878C= ENSP00000361287.3:p.Ser293=
ENST00000480845.1:n.110C=
ENST00000485270.5:n.390C=
NM_000429.2:c.878C= NP_000420.1:p.Ser293=
XM_005269842.3:c.878C= XP_005269899.1:p.Ser293=
XM_005269843.3:c.755C= XP_005269900.1:p.Ser252=
NM_000429.3:c.878C= MANE Select NP_000420.1:p.Ser293=