Canonical Allele Identifier: CA2582641924
Gene: GAMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1401407del , CM000681.2:g.1401407del GRCh38
NC_000019.9:g.1401406del , CM000681.1:g.1401406del GRCh37
NC_000019.8:g.1352406del NCBI36
NG_009785.1:g.5149del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252288.8:c.72del MANE Select ENSP00000252288.1:p.Ala25ArgfsTer17
ENST00000447102.8:c.72del ENSP00000403536.2:p.Ala25ArgfsTer17
ENST00000640762.1:c.72del ENSP00000492031.1:p.Ala25ArgfsTer?
ENST00000252288.6:c.72del ENSP00000252288.1:p.Ala25ArgfsTer17
ENST00000447102.7:c.72del ENSP00000403536.2:p.Ala25ArgfsTer17
NM_000156.5:c.72del NP_000147.1:p.Ala25ArgfsTer17
NM_138924.2:c.72del NP_620279.1:p.Ala25ArgfsTer17
NM_000156.6:c.72del MANE Select NP_000147.1:p.Ala25ArgfsTer17
NM_138924.3:c.72del NP_620279.1:p.Ala25ArgfsTer17