Canonical Allele Identifier: CA402996278
Gene: GAMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1399828G>C , CM000681.2:g.1399828G>C GRCh38
NC_000019.9:g.1399827G>C , CM000681.1:g.1399827G>C GRCh37
NC_000019.8:g.1350827G>C NCBI36
NG_009785.1:g.6726C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.292C>G MANE Select ENSP00000252288.1:p.Arg98Gly
ENST00000447102.8:c.292C>G ENSP00000403536.2:p.Arg98Gly
ENST00000640762.1:c.223C>G ENSP00000492031.1:p.Arg75Gly
ENST00000252288.6:c.292C>G ENSP00000252288.1:p.Arg98Gly
ENST00000447102.7:c.292C>G ENSP00000403536.2:p.Arg98Gly
NM_000156.5:c.292C>G NP_000147.1:p.Arg98Gly
NM_138924.2:c.292C>G NP_620279.1:p.Arg98Gly
NM_000156.6:c.292C>G MANE Select NP_000147.1:p.Arg98Gly
NM_138924.3:c.292C>G NP_620279.1:p.Arg98Gly