Canonical Allele Identifier: CA2575525319
Gene: PYGL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50915881_50915912del , CM000676.2:g.50915881_50915912del GRCh38
NC_000014.8:g.51382599_51382630del , CM000676.1:g.51382599_51382630del GRCh37
NC_000014.7:g.50452349_50452380del NCBI36
NG_012796.1:g.33619_33650del

Transcript Alleles

HGVS Amino-acid change
ENST00000216392.8:c.1152_1183del MANE Select ENSP00000216392.7:p.Leu385AlafsTer11
ENST00000216392.7:c.1152_1183del ENSP00000216392.7:p.Leu385AlafsTer11
ENST00000528757.2:n.29_60del
ENST00000532462.5:c.1152_1183del ENSP00000431657.1:p.Leu385AlafsTer11
ENST00000544180.6:c.1050_1081del ENSP00000443787.1:p.Leu351AlafsTer11
NM_001163940.1:c.1050_1081del NP_001157412.1:p.Leu351AlafsTer11
NM_002863.4:c.1152_1183del NP_002854.3:p.Leu385AlafsTer11
NM_002863.5:c.1152_1183del MANE Select NP_002854.3:p.Leu385AlafsTer11
NM_001163940.2:c.1050_1081del NP_001157412.1:p.Leu351AlafsTer11