Canonical Allele Identifier: CA389699091

Gene: PYGL

Linked Data

• gnomAD v4: 14-50944166-G-T
• MyVariant Identifiers: chr14:g.51410884G>T (hg19) ; chr14:g.50944166G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50944166G>T , CM000676.2:g.50944166G>T	GRCh38
NC_000014.8:g.51410884G>T , CM000676.1:g.51410884G>T	GRCh37
NC_000014.7:g.50480634G>T	NCBI36
NG_012796.1:g.5365C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216392.8:c.238C>A MANE Select	ENSP00000216392.7:p.Pro80Thr
ENST00000216392.7:c.238C>A	ENSP00000216392.7:p.Pro80Thr
ENST00000530336.2:n.305C>A
ENST00000532462.5:c.238C>A	ENSP00000431657.1:p.Pro80Thr
ENST00000544180.6:c.238C>A	ENSP00000443787.1:p.Pro80Thr
NM_001163940.1:c.238C>A	NP_001157412.1:p.Pro80Thr
NM_002863.4:c.238C>A	NP_002854.3:p.Pro80Thr
NM_002863.5:c.238C>A MANE Select	NP_002854.3:p.Pro80Thr
NM_001163940.2:c.238C>A	NP_001157412.1:p.Pro80Thr