Canonical Allele Identifier: CA389683143

Gene: PYGL

Linked Data

• MyVariant Identifiers: chr14:g.51378476C>A (hg19) ; chr14:g.50911758C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50911758C>A , CM000676.2:g.50911758C>A	GRCh38
NC_000014.8:g.51378476C>A , CM000676.1:g.51378476C>A	GRCh37
NC_000014.7:g.50448226C>A	NCBI36
NG_012796.1:g.37773G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216392.8:c.1941G>T MANE Select	ENSP00000216392.7:p.Glu647Asp
ENST00000216392.7:c.1941G>T	ENSP00000216392.7:p.Glu647Asp
ENST00000532107.2:n.114G>T
ENST00000532462.5:c.1941G>T	ENSP00000431657.1:p.Glu647Asp
ENST00000544180.6:c.1839G>T	ENSP00000443787.1:p.Glu613Asp
NM_001163940.1:c.1839G>T	NP_001157412.1:p.Glu613Asp
NM_002863.4:c.1941G>T	NP_002854.3:p.Glu647Asp
NM_002863.5:c.1941G>T MANE Select	NP_002854.3:p.Glu647Asp
NM_001163940.2:c.1839G>T	NP_001157412.1:p.Glu613Asp