Canonical Allele Identifier: CA2801553804
Gene: PYGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50905359del , CM000676.2:g.50905359del GRCh38
NC_000014.8:g.51372077del , CM000676.1:g.51372077del GRCh37
NC_000014.7:g.50441827del NCBI36
NG_012796.1:g.44173del

Transcript Alleles

HGVS Amino-acid Change
ENST00000216392.8:c.*34del MANE Select ENSP00000216392.7:n.*34del
ENST00000216392.7:c.*34del ENSP00000216392.7:n.*34del
ENST00000532462.5:c.2379+2913del ENSP00000431657.1:n.2379+2913del
ENST00000544180.6:c.*34del ENSP00000443787.1:n.*34del
NM_001163940.1:c.*34del NP_001157412.1:n.*34del
NM_002863.4:c.*34del NP_002854.3:n.*34del
NM_002863.5:c.*34del MANE Select NP_002854.3:n.*34del
NM_001163940.2:c.*34del NP_001157412.1:n.*34del