Canonical Allele Identifier: CA504895115
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1101809
ClinVar RCV Id: RCV001424905
dbSNP Id: rs2144636311
gnomAD v4: 19-1398970-G-T
MyVariant Identifiers: chr19:g.1398969G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1398970G>T , CM000681.2:g.1398970G>T GRCh38
NC_000019.9:g.1398969G>T , CM000681.1:g.1398969G>T GRCh37
NC_000019.8:g.1349969G>T NCBI36
NG_009785.1:g.7584C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.516C>A MANE Select ENSP00000252288.1:p.Thr172=
ENST00000447102.8:c.516C>A ENSP00000403536.2:p.Thr172=
ENST00000591788.3:c.199C>A
ENST00000640164.1:n.349C>A
ENST00000640762.1:c.447C>A ENSP00000492031.1:p.Thr149=
ENST00000252288.6:c.516C>A ENSP00000252288.1:p.Thr172=
ENST00000447102.7:c.516C>A ENSP00000403536.2:p.Thr172=
ENST00000591788.2:c.201C>A ENSP00000466341.2:p.Thr67=
NM_000156.5:c.516C>A NP_000147.1:p.Thr172=
NM_138924.2:c.516C>A NP_620279.1:p.Thr172=
NM_000156.6:c.516C>A MANE Select NP_000147.1:p.Thr172=
NM_138924.3:c.516C>A NP_620279.1:p.Thr172=