Canonical Allele Identifier: CA1922573369
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80275083T= , CM000672.2:g.80275083T= GRCh38
NC_000010.10:g.82034839T= , CM000672.1:g.82034839T= GRCh37
NC_000010.9:g.82024819T= NCBI36
NG_008083.1:g.19596A=

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.885A= MANE Select ENSP00000361287.3:p.Ala295=
ENST00000372213.7:c.885A= ENSP00000361287.3:p.Ala295=
ENST00000480845.1:n.117A=
ENST00000485270.5:n.397A=
NM_000429.2:c.885A= NP_000420.1:p.Ala295=
XM_005269842.3:c.885A= XP_005269899.1:p.Ala295=
XM_005269843.3:c.762A= XP_005269900.1:p.Ala254=
NM_000429.3:c.885A= MANE Select NP_000420.1:p.Ala295=