Canonical Allele Identifier: CA504731734
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2811055
ClinVar RCV Id: RCV003746983
dbSNP Id: rs1262796024
gnomAD v2: 19-1401437-G-C
gnomAD v3: 19-1401438-G-C
gnomAD v4: 19-1401438-G-C

Genomic Alleles

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

Transcript Alleles

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