Canonical Allele Identifier: CA1922577921
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80274605T= , CM000672.2:g.80274605T= GRCh38
NC_000010.10:g.82034361T= , CM000672.1:g.82034361T= GRCh37
NC_000010.9:g.82024341T= NCBI36
NG_008083.1:g.20074A=

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.1000A= MANE Select ENSP00000361287.3:p.Thr334=
ENST00000372213.7:c.1000A= ENSP00000361287.3:p.Thr334=
ENST00000480845.1:n.232A=
ENST00000485270.5:n.512A=
NM_000429.2:c.1000A= NP_000420.1:p.Thr334=
XM_005269842.3:c.1000A= XP_005269899.1:p.Thr334=
XM_005269843.3:c.877A= XP_005269900.1:p.Thr293=
NM_000429.3:c.1000A= MANE Select NP_000420.1:p.Thr334=