Canonical Allele Identifier: CA314789
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 205571
ClinVar RCV Id: RCV000187554
dbSNP Id: rs578080158
gnomAD v2: 19-1401506-T-C
gnomAD v3: 19-1401507-T-C
gnomAD v4: 19-1401507-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401507T>C , CM000681.2:g.1401507T>C GRCh38
NC_000019.9:g.1401506T>C , CM000681.1:g.1401506T>C GRCh37
NC_000019.8:g.1352506T>C NCBI36
NG_009785.1:g.5047A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.-31A>G MANE Select ENSP00000252288.1:n.-31A>G
ENST00000447102.8:c.-31A>G ENSP00000403536.2:n.-31A>G
ENST00000252288.6:c.-31A>G ENSP00000252288.1:n.-31A>G
ENST00000447102.7:c.-31A>G ENSP00000403536.2:n.-31A>G
NM_000156.5:c.-31A>G NP_000147.1:n.-31A>G
NM_138924.2:c.-31A>G NP_620279.1:n.-31A>G
NM_000156.6:c.-31A>G MANE Select NP_000147.1:n.-31A>G
NM_138924.3:c.-31A>G NP_620279.1:n.-31A>G