Canonical Allele Identifier: CA1922577116
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80273765C= , CM000672.2:g.80273765C= GRCh38
NC_000010.10:g.82033521C= , CM000672.1:g.82033521C= GRCh37
NC_000010.9:g.82023501C= NCBI36
NG_008083.1:g.20914G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.*16G= MANE Select ENSP00000361287.3:n.*16G=
ENST00000372213.7:c.*16G= ENSP00000361287.3:n.*16G=
ENST00000480845.1:n.436G=
ENST00000485270.5:n.716G=
NM_000429.2:c.*16G= NP_000420.1:n.*16G=
XM_005269842.3:c.*16G= XP_005269899.1:n.*16G=
XM_005269843.3:c.*16G= XP_005269900.1:n.*16G=
NM_000429.3:c.*16G= MANE Select NP_000420.1:n.*16G=