Canonical Allele Identifier: CA504895133
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 506679
dbSNP Id: rs1555777024
gnomAD v3: 19-1398979-G-A
gnomAD v4: 19-1398979-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1398979G>A , CM000681.2:g.1398979G>A GRCh38
NC_000019.9:g.1398978G>A , CM000681.1:g.1398978G>A GRCh37
NC_000019.8:g.1349978G>A NCBI36
NG_009785.1:g.7575C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.507C>T MANE Select ENSP00000252288.1:p.Cys169=
ENST00000447102.8:c.507C>T ENSP00000403536.2:p.Cys169=
ENST00000591788.3:c.190C>T
ENST00000640164.1:n.340C>T
ENST00000640762.1:c.438C>T ENSP00000492031.1:p.Cys146=
ENST00000252288.6:c.507C>T ENSP00000252288.1:p.Cys169=
ENST00000447102.7:c.507C>T ENSP00000403536.2:p.Cys169=
ENST00000591788.2:c.192C>T ENSP00000466341.2:p.Cys64=
NM_000156.5:c.507C>T NP_000147.1:p.Cys169=
NM_138924.2:c.507C>T NP_620279.1:p.Cys169=
NM_000156.6:c.507C>T MANE Select NP_000147.1:p.Cys169=
NM_138924.3:c.507C>T NP_620279.1:p.Cys169=