Canonical Allele Identifier: CA9043792
Gene: GAMT HGNC NCBI

Linked Data

dbSNP Id: rs773832312
gnomAD v2: 19-1401303-G-A
gnomAD v4: 19-1401304-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401304G>A , CM000681.2:g.1401304G>A GRCh38
NC_000019.9:g.1401303G>A , CM000681.1:g.1401303G>A GRCh37
NC_000019.8:g.1352303G>A NCBI36
NG_009785.1:g.5250C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.173C>T MANE Select ENSP00000252288.1:p.Ser58Phe
ENST00000447102.8:c.173C>T ENSP00000403536.2:p.Ser58Phe
ENST00000640762.1:c.112+61C>T ENSP00000492031.1:n.112+61C>T
ENST00000252288.6:c.173C>T ENSP00000252288.1:p.Ser58Phe
ENST00000447102.7:c.173C>T ENSP00000403536.2:p.Ser58Phe
NM_000156.5:c.173C>T NP_000147.1:p.Ser58Phe
NM_138924.2:c.173C>T NP_620279.1:p.Ser58Phe
NM_000156.6:c.173C>T MANE Select NP_000147.1:p.Ser58Phe
NM_138924.3:c.173C>T NP_620279.1:p.Ser58Phe