Canonical Allele Identifier: CA658799100
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 518184
ClinVar RCV Id: RCV000609293
dbSNP Id: rs1555777388
gnomAD v4: 19-1401484-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401484G>C , CM000681.2:g.1401484G>C GRCh38
NC_000019.9:g.1401483G>C , CM000681.1:g.1401483G>C GRCh37
NC_000019.8:g.1352483G>C NCBI36
NG_009785.1:g.5070C>G

Transcript Alleles

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