Canonical Allele Identifier: CA314790
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 205572
ClinVar RCV Id: RCV000187555
dbSNP Id: rs796052521
gnomAD v2: 19-1401502-T-G
gnomAD v3: 19-1401503-T-G
gnomAD v4: 19-1401503-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401503T>G , CM000681.2:g.1401503T>G GRCh38
NC_000019.9:g.1401502T>G , CM000681.1:g.1401502T>G GRCh37
NC_000019.8:g.1352502T>G NCBI36
NG_009785.1:g.5051A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.-27A>C MANE Select ENSP00000252288.1:n.-27A>C
ENST00000447102.8:c.-27A>C ENSP00000403536.2:n.-27A>C
ENST00000252288.6:c.-27A>C ENSP00000252288.1:n.-27A>C
ENST00000447102.7:c.-27A>C ENSP00000403536.2:n.-27A>C
NM_000156.5:c.-27A>C NP_000147.1:n.-27A>C
NM_138924.2:c.-27A>C NP_620279.1:n.-27A>C
NM_000156.6:c.-27A>C MANE Select NP_000147.1:n.-27A>C
NM_138924.3:c.-27A>C NP_620279.1:n.-27A>C