Canonical Allele Identifier: CA1922573388
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275089T= , CM000672.2:g.80275089T= GRCh38
NC_000010.10:g.82034845T= , CM000672.1:g.82034845T= GRCh37
NC_000010.9:g.82024825T= NCBI36
NG_008083.1:g.19590A=

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.879A= MANE Select ENSP00000361287.3:p.Ser293=
ENST00000372213.7:c.879A= ENSP00000361287.3:p.Ser293=
ENST00000480845.1:n.111A=
ENST00000485270.5:n.391A=
NM_000429.2:c.879A= NP_000420.1:p.Ser293=
XM_005269842.3:c.879A= XP_005269899.1:p.Ser293=
XM_005269843.3:c.756A= XP_005269900.1:p.Ser252=
NM_000429.3:c.879A= MANE Select NP_000420.1:p.Ser293=