Canonical Allele Identifier: CA2136411058
Gene: PYGL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50905315A= , CM000676.2:g.50905315A= GRCh38
NC_000014.8:g.51372033A= , CM000676.1:g.51372033A= GRCh37
NC_000014.7:g.50441783A= NCBI36
NG_012796.1:g.44216T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216392.8:c.*77T= MANE Select ENSP00000216392.7:n.*77T=
ENST00000216392.7:c.*77T= ENSP00000216392.7:n.*77T=
ENST00000532462.5:c.2379+2956T= ENSP00000431657.1:n.2379+2956T=
ENST00000544180.6:c.*77T= ENSP00000443787.1:n.*77T=
NM_001163940.1:c.*77T= NP_001157412.1:n.*77T=
NM_002863.4:c.*77T= NP_002854.3:n.*77T=
NM_002863.5:c.*77T= MANE Select NP_002854.3:n.*77T=
NM_001163940.2:c.*77T= NP_001157412.1:n.*77T=
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