Canonical Allele Identifier: CA9043812
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1145657
ClinVar RCV Id: RCV001484571
dbSNP Id: rs763777192
gnomAD v2: 19-1401443-C-A
gnomAD v3: 19-1401444-C-A
gnomAD v4: 19-1401444-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401444C>A , CM000681.2:g.1401444C>A GRCh38
NC_000019.9:g.1401443C>A , CM000681.1:g.1401443C>A GRCh37
NC_000019.8:g.1352443C>A NCBI36
NG_009785.1:g.5110G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.33G>T MANE Select ENSP00000252288.1:p.Ala11=
ENST00000447102.8:c.33G>T ENSP00000403536.2:p.Ala11=
ENST00000640762.1:c.33G>T ENSP00000492031.1:p.Ala11=
ENST00000252288.6:c.33G>T ENSP00000252288.1:p.Ala11=
ENST00000447102.7:c.33G>T ENSP00000403536.2:p.Ala11=
NM_000156.5:c.33G>T NP_000147.1:p.Ala11=
NM_138924.2:c.33G>T NP_620279.1:p.Ala11=
NM_000156.6:c.33G>T MANE Select NP_000147.1:p.Ala11=
NM_138924.3:c.33G>T NP_620279.1:p.Ala11=