Canonical Allele Identifier: CA1922577119
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80273769C= , CM000672.2:g.80273769C= GRCh38
NC_000010.10:g.82033525C= , CM000672.1:g.82033525C= GRCh37
NC_000010.9:g.82023505C= NCBI36
NG_008083.1:g.20910G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.*12G= MANE Select ENSP00000361287.3:n.*12G=
ENST00000372213.7:c.*12G= ENSP00000361287.3:n.*12G=
ENST00000480845.1:n.432G=
ENST00000485270.5:n.712G=
NM_000429.2:c.*12G= NP_000420.1:n.*12G=
XM_005269842.3:c.*12G= XP_005269899.1:n.*12G=
XM_005269843.3:c.*12G= XP_005269900.1:n.*12G=
NM_000429.3:c.*12G= MANE Select NP_000420.1:n.*12G=