Canonical Allele Identifier: CA1922577176
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80273808C= , CM000672.2:g.80273808C= GRCh38
NC_000010.10:g.82033564C= , CM000672.1:g.82033564C= GRCh37
NC_000010.9:g.82023544C= NCBI36
NG_008083.1:g.20871G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.1161G= MANE Select ENSP00000361287.3:p.Trp387=
ENST00000372213.7:c.1161G= ENSP00000361287.3:p.Trp387=
ENST00000480845.1:n.393G=
ENST00000485270.5:n.673G=
NM_000429.2:c.1161G= NP_000420.1:p.Trp387=
XM_005269842.3:c.1161G= XP_005269899.1:p.Trp387=
XM_005269843.3:c.1038G= XP_005269900.1:p.Trp346=
NM_000429.3:c.1161G= MANE Select NP_000420.1:p.Trp387=