Canonical Allele Identifier: CA2624828823

Gene: PYGL

Linked Data

• gnomAD v4: 14-50905333-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50905333T>A , CM000676.2:g.50905333T>A	GRCh38
NC_000014.8:g.51372051T>A , CM000676.1:g.51372051T>A	GRCh37
NC_000014.7:g.50441801T>A	NCBI36
NG_012796.1:g.44198A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216392.8:c.*59A>T MANE Select	ENSP00000216392.7:n.*59A>T
ENST00000216392.7:c.*59A>T	ENSP00000216392.7:n.*59A>T
ENST00000532462.5:c.2379+2938A>T	ENSP00000431657.1:n.2379+2938A>T
ENST00000544180.6:c.*59A>T	ENSP00000443787.1:n.*59A>T
NM_001163940.1:c.*59A>T	NP_001157412.1:n.*59A>T
NM_002863.4:c.*59A>T	NP_002854.3:n.*59A>T
NM_002863.5:c.*59A>T MANE Select	NP_002854.3:n.*59A>T
NM_001163940.2:c.*59A>T	NP_001157412.1:n.*59A>T