Canonical Allele Identifier: CA2614191700
Gene: PYGM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64759676_64759678del , CM000673.2:g.64759676_64759678del GRCh38
NC_000011.9:g.64527148_64527150del , CM000673.1:g.64527148_64527150del GRCh37
NC_000011.8:g.64283724_64283726del NCBI36
NG_013018.1:g.6042_6044del

Transcript Alleles

HGVS Amino-acid Change
ENST00000164139.4:c.225_227del MANE Select ENSP00000164139.3:p.Tyr76del
ENST00000164139.3:c.225_227del ENSP00000164139.3:p.Tyr76del
ENST00000377432.7:c.225_227del ENSP00000366650.3:p.Tyr76del
NM_001164716.1:c.225_227del NP_001158188.1:p.Tyr76del
NM_005609.2:c.225_227del NP_005600.1:p.Tyr76del
NM_005609.3:c.225_227del NP_005600.1:p.Tyr76del
NM_005609.4:c.225_227del MANE Select NP_005600.1:p.Tyr76del