Canonical Allele Identifier: CA389683016

Gene: PYGL

Linked Data

• COSMIC: COSM3711569
• MyVariant Identifiers: chr14:g.51378457C>T (hg19) ; chr14:g.50911739C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50911739C>T , CM000676.2:g.50911739C>T	GRCh38
NC_000014.8:g.51378457C>T , CM000676.1:g.51378457C>T	GRCh37
NC_000014.7:g.50448207C>T	NCBI36
NG_012796.1:g.37792G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216392.8:c.1960G>A MANE Select	ENSP00000216392.7:p.Ala654Thr
ENST00000216392.7:c.1960G>A	ENSP00000216392.7:p.Ala654Thr
ENST00000532107.2:n.133G>A
ENST00000532462.5:c.1960G>A	ENSP00000431657.1:p.Ala654Thr
ENST00000544180.6:c.1858G>A	ENSP00000443787.1:p.Ala620Thr
NM_001163940.1:c.1858G>A	NP_001157412.1:p.Ala620Thr
NM_002863.4:c.1960G>A	NP_002854.3:p.Ala654Thr
NM_002863.5:c.1960G>A MANE Select	NP_002854.3:p.Ala654Thr
NM_001163940.2:c.1858G>A	NP_001157412.1:p.Ala620Thr