Canonical Allele Identifier: CA2574864852
Gene: PYGM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64758513del , CM000673.2:g.64758513del GRCh38
NC_000011.9:g.64525985del , CM000673.1:g.64525985del GRCh37
NC_000011.8:g.64282561del NCBI36
NG_013018.1:g.7205del

Transcript Alleles

HGVS Amino-acid change
ENST00000164139.4:c.350del MANE Select ENSP00000164139.3:p.Gly117AlafsTer?
ENST00000164139.3:c.350del ENSP00000164139.3:p.Gly117AlafsTer?
ENST00000377432.7:c.244-245del ENSP00000366650.3:n.244-245del
NM_001164716.1:c.244-245del NP_001158188.1:n.244-245del
NM_005609.2:c.350del NP_005600.1:p.Gly117AlafsTer?
NM_005609.3:c.350del NP_005600.1:p.Gly117AlafsTer?
NM_005609.4:c.350del MANE Select NP_005600.1:p.Gly117AlafsTer?