Canonical Allele Identifier: CA504731733
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 839981
ClinVar RCV Id: RCV001041865
dbSNP Id: rs1262796024
gnomAD v2: 19-1401437-G-A
gnomAD v4: 19-1401438-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401438G>A , CM000681.2:g.1401438G>A GRCh38
NC_000019.9:g.1401437G>A , CM000681.1:g.1401437G>A GRCh37
NC_000019.8:g.1352437G>A NCBI36
NG_009785.1:g.5116C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.39C>T MANE Select ENSP00000252288.1:p.Gly13=
ENST00000447102.8:c.39C>T ENSP00000403536.2:p.Gly13=
ENST00000640762.1:c.39C>T ENSP00000492031.1:p.Gly13=
ENST00000252288.6:c.39C>T ENSP00000252288.1:p.Gly13=
ENST00000447102.7:c.39C>T ENSP00000403536.2:p.Gly13=
NM_000156.5:c.39C>T NP_000147.1:p.Gly13=
NM_138924.2:c.39C>T NP_620279.1:p.Gly13=
NM_000156.6:c.39C>T MANE Select NP_000147.1:p.Gly13=
NM_138924.3:c.39C>T NP_620279.1:p.Gly13=