Canonical Allele Identifier: CA1922573366
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275082A= , CM000672.2:g.80275082A= GRCh38
NC_000010.10:g.82034838A= , CM000672.1:g.82034838A= GRCh37
NC_000010.9:g.82024818A= NCBI36
NG_008083.1:g.19597T=

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.886T= MANE Select ENSP00000361287.3:p.Tyr296=
ENST00000372213.7:c.886T= ENSP00000361287.3:p.Tyr296=
ENST00000480845.1:n.118T=
ENST00000485270.5:n.398T=
NM_000429.2:c.886T= NP_000420.1:p.Tyr296=
XM_005269842.3:c.886T= XP_005269899.1:p.Tyr296=
XM_005269843.3:c.763T= XP_005269900.1:p.Tyr255=
NM_000429.3:c.886T= MANE Select NP_000420.1:p.Tyr296=