Canonical Allele Identifier: CA504895121
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 765882
ClinVar RCV Id: RCV001466758
dbSNP Id: rs748417607
gnomAD v4: 19-1398973-G-A
MyVariant Identifiers: chr19:g.1398972G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1398973G>A , CM000681.2:g.1398973G>A GRCh38
NC_000019.9:g.1398972G>A , CM000681.1:g.1398972G>A GRCh37
NC_000019.8:g.1349972G>A NCBI36
NG_009785.1:g.7581C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.513C>T MANE Select ENSP00000252288.1:p.Leu171=
ENST00000447102.8:c.513C>T ENSP00000403536.2:p.Leu171=
ENST00000591788.3:c.196C>T
ENST00000640164.1:n.346C>T
ENST00000640762.1:c.444C>T ENSP00000492031.1:p.Leu148=
ENST00000252288.6:c.513C>T ENSP00000252288.1:p.Leu171=
ENST00000447102.7:c.513C>T ENSP00000403536.2:p.Leu171=
ENST00000591788.2:c.198C>T ENSP00000466341.2:p.Leu66=
NM_000156.5:c.513C>T NP_000147.1:p.Leu171=
NM_138924.2:c.513C>T NP_620279.1:p.Leu171=
NM_000156.6:c.513C>T MANE Select NP_000147.1:p.Leu171=
NM_138924.3:c.513C>T NP_620279.1:p.Leu171=