Canonical Allele Identifier: CA10651555
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 328353
ClinVar RCV Id: RCV000295163 RCV000519834 RCV001859934
dbSNP Id: rs886054248
gnomAD v2: 19-1401412-C-T
gnomAD v3: 19-1401413-C-T
gnomAD v4: 19-1401413-C-T
MyVariant Identifiers: chr19:g.1401412C>T (hg19) chr19:g.1401413C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401413C>T , CM000681.2:g.1401413C>T GRCh38
NC_000019.9:g.1401412C>T , CM000681.1:g.1401412C>T GRCh37
NC_000019.8:g.1352412C>T NCBI36
NG_009785.1:g.5141G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000252288.8:c.64G>A MANE Select ENSP00000252288.1:p.Ala22Thr
ENST00000447102.8:c.64G>A ENSP00000403536.2:p.Ala22Thr
ENST00000640762.1:c.64G>A ENSP00000492031.1:p.Ala22Thr
ENST00000252288.6:c.64G>A ENSP00000252288.1:p.Ala22Thr
ENST00000447102.7:c.64G>A ENSP00000403536.2:p.Ala22Thr
NM_000156.5:c.64G>A NP_000147.1:p.Ala22Thr
NM_138924.2:c.64G>A NP_620279.1:p.Ala22Thr
NM_000156.6:c.64G>A MANE Select NP_000147.1:p.Ala22Thr
NM_138924.3:c.64G>A NP_620279.1:p.Ala22Thr
Search 100 bp 5'
Search 100 bp 3'