Canonical Allele Identifier: CA2136411087
Gene: PYGL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50905353T= , CM000676.2:g.50905353T= GRCh38
NC_000014.8:g.51372071T= , CM000676.1:g.51372071T= GRCh37
NC_000014.7:g.50441821T= NCBI36
NG_012796.1:g.44178A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216392.8:c.*39A= MANE Select ENSP00000216392.7:n.*39A=
ENST00000216392.7:c.*39A= ENSP00000216392.7:n.*39A=
ENST00000532462.5:c.2379+2918A= ENSP00000431657.1:n.2379+2918A=
ENST00000544180.6:c.*39A= ENSP00000443787.1:n.*39A=
NM_001163940.1:c.*39A= NP_001157412.1:n.*39A=
NM_002863.4:c.*39A= NP_002854.3:n.*39A=
NM_002863.5:c.*39A= MANE Select NP_002854.3:n.*39A=
NM_001163940.2:c.*39A= NP_001157412.1:n.*39A=
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