Canonical Allele Identifier: CA504731758
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 2098482
ClinVar RCV Id: RCV003008469
gnomAD v4: 19-1401459-C-T
MyVariant Identifiers: chr19:g.1401458C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401459C>T , CM000681.2:g.1401459C>T GRCh38
NC_000019.9:g.1401458C>T , CM000681.1:g.1401458C>T GRCh37
NC_000019.8:g.1352458C>T NCBI36
NG_009785.1:g.5095G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.18G>A MANE Select ENSP00000252288.1:p.Ala6=
ENST00000447102.8:c.18G>A ENSP00000403536.2:p.Ala6=
ENST00000640762.1:c.18G>A ENSP00000492031.1:p.Ala6=
ENST00000252288.6:c.18G>A ENSP00000252288.1:p.Ala6=
ENST00000447102.7:c.18G>A ENSP00000403536.2:p.Ala6=
NM_000156.5:c.18G>A NP_000147.1:p.Ala6=
NM_138924.2:c.18G>A NP_620279.1:p.Ala6=
NM_000156.6:c.18G>A MANE Select NP_000147.1:p.Ala6=
NM_138924.3:c.18G>A NP_620279.1:p.Ala6=