Canonical Allele Identifier: CA1922577081
Gene: MAT1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80273743T= , CM000672.2:g.80273743T= GRCh38
NC_000010.10:g.82033499T= , CM000672.1:g.82033499T= GRCh37
NC_000010.9:g.82023479T= NCBI36
NG_008083.1:g.20936A=

Transcript Alleles

HGVS Amino-acid change
ENST00000372213.8:c.*38A= MANE Select ENSP00000361287.3:n.*38A=
ENST00000372213.7:c.*38A= ENSP00000361287.3:n.*38A=
ENST00000480845.1:n.458A=
ENST00000485270.5:n.738A=
NM_000429.2:c.*38A= NP_000420.1:n.*38A=
XM_005269842.3:c.*38A= XP_005269899.1:n.*38A=
XM_005269843.3:c.*38A= XP_005269900.1:n.*38A=
NM_000429.3:c.*38A= MANE Select NP_000420.1:n.*38A=