Canonical Allele Identifier: CA1922577166
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80273799G= , CM000672.2:g.80273799G= GRCh38
NC_000010.10:g.82033555G= , CM000672.1:g.82033555G= GRCh37
NC_000010.9:g.82023535G= NCBI36
NG_008083.1:g.20880C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.1170C= MANE Select ENSP00000361287.3:p.Pro390=
ENST00000372213.7:c.1170C= ENSP00000361287.3:p.Pro390=
ENST00000480845.1:n.402C=
ENST00000485270.5:n.682C=
NM_000429.2:c.1170C= NP_000420.1:p.Pro390=
XM_005269842.3:c.1170C= XP_005269899.1:p.Pro390=
XM_005269843.3:c.1047C= XP_005269900.1:p.Pro349=
NM_000429.3:c.1170C= MANE Select NP_000420.1:p.Pro390=