Canonical Allele Identifier: CA2624831836

Gene: PYGL

Linked Data

• gnomAD v4: 14-50915792-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50915792C>A , CM000676.2:g.50915792C>A	GRCh38
NC_000014.8:g.51382510C>A , CM000676.1:g.51382510C>A	GRCh37
NC_000014.7:g.50452260C>A	NCBI36
NG_012796.1:g.33739G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000216392.8:c.1239+33G>T MANE Select	ENSP00000216392.7:n.1239+33G>T
ENST00000216392.7:c.1239+33G>T	ENSP00000216392.7:n.1239+33G>T
ENST00000528757.2:n.116+33G>T
ENST00000532462.5:c.1239+33G>T	ENSP00000431657.1:n.1239+33G>T
ENST00000544180.6:c.1137+33G>T	ENSP00000443787.1:n.1137+33G>T
NM_001163940.1:c.1137+33G>T	NP_001157412.1:n.1137+33G>T
NM_002863.4:c.1239+33G>T	NP_002854.3:n.1239+33G>T
NM_002863.5:c.1239+33G>T MANE Select	NP_002854.3:n.1239+33G>T
NM_001163940.2:c.1137+33G>T	NP_001157412.1:n.1137+33G>T