Canonical Allele Identifier: CA389678763

Gene: PYGL

Linked Data

• dbSNP Id: rs1419703214
• gnomAD v3: 14-50905423-G-T
• gnomAD v4: 14-50905423-G-T
• MyVariant Identifiers: chr14:g.51372141G>T (hg19) ; chr14:g.50905423G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50905423G>T , CM000676.2:g.50905423G>T	GRCh38
NC_000014.8:g.51372141G>T , CM000676.1:g.51372141G>T	GRCh37
NC_000014.7:g.50441891G>T	NCBI36
NG_012796.1:g.44108C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216392.8:c.2513C>A MANE Select	ENSP00000216392.7:p.Ser838Tyr
ENST00000216392.7:c.2513C>A	ENSP00000216392.7:p.Ser838Tyr
ENST00000532462.5:c.2379+2848C>A	ENSP00000431657.1:n.2379+2848C>A
ENST00000544180.6:c.2411C>A	ENSP00000443787.1:p.Ser804Tyr
NM_001163940.1:c.2411C>A	NP_001157412.1:p.Ser804Tyr
NM_002863.4:c.2513C>A	NP_002854.3:p.Ser838Tyr
NM_002863.5:c.2513C>A MANE Select	NP_002854.3:p.Ser838Tyr
NM_001163940.2:c.2411C>A	NP_001157412.1:p.Ser804Tyr