Canonical Allele Identifier: CA1922577118
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80273768G= , CM000672.2:g.80273768G= GRCh38
NC_000010.10:g.82033524G= , CM000672.1:g.82033524G= GRCh37
NC_000010.9:g.82023504G= NCBI36
NG_008083.1:g.20911C=

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.*13C= MANE Select ENSP00000361287.3:n.*13C=
ENST00000372213.7:c.*13C= ENSP00000361287.3:n.*13C=
ENST00000480845.1:n.433C=
ENST00000485270.5:n.713C=
NM_000429.2:c.*13C= NP_000420.1:n.*13C=
XM_005269842.3:c.*13C= XP_005269899.1:n.*13C=
XM_005269843.3:c.*13C= XP_005269900.1:n.*13C=
NM_000429.3:c.*13C= MANE Select NP_000420.1:n.*13C=