Canonical Allele Identifier: CA504730083
Gene: GAMT HGNC NCBI

Linked Data

dbSNP Id: rs80338733
gnomAD v2: 19-1399148-T-A
gnomAD v4: 19-1399149-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399149T>A , CM000681.2:g.1399149T>A GRCh38
NC_000019.9:g.1399148T>A , CM000681.1:g.1399148T>A GRCh37
NC_000019.8:g.1350148T>A NCBI36
NG_009785.1:g.7405A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.438A>T MANE Select ENSP00000252288.1:p.Thr146=
ENST00000447102.8:c.438A>T ENSP00000403536.2:p.Thr146=
ENST00000591788.3:c.121A>T
ENST00000640164.1:n.271A>T
ENST00000640762.1:c.369A>T ENSP00000492031.1:p.Thr123=
ENST00000252288.6:c.438A>T ENSP00000252288.1:p.Thr146=
ENST00000447102.7:c.438A>T ENSP00000403536.2:p.Thr146=
ENST00000591788.2:c.123A>T ENSP00000466341.2:p.Thr41=
NM_000156.5:c.438A>T NP_000147.1:p.Thr146=
NM_138924.2:c.438A>T NP_620279.1:p.Thr146=
NM_000156.6:c.438A>T MANE Select NP_000147.1:p.Thr146=
NM_138924.3:c.438A>T NP_620279.1:p.Thr146=