Canonical Allele Identifier: CA389699746

Gene: PYGL

Linked Data

• dbSNP Id: rs758520596
• COSMIC: COSM1640102
• MyVariant Identifiers: chr14:g.51411091G>A (hg19) ; chr14:g.50944373G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50944373G>A , CM000676.2:g.50944373G>A	GRCh38
NC_000014.8:g.51411091G>A , CM000676.1:g.51411091G>A	GRCh37
NC_000014.7:g.50480841G>A	NCBI36
NG_012796.1:g.5158C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000216392.8:c.31C>T MANE Select	ENSP00000216392.7:p.Arg11Trp
ENST00000216392.7:c.31C>T	ENSP00000216392.7:p.Arg11Trp
ENST00000530336.2:n.98C>T
ENST00000532462.5:c.31C>T	ENSP00000431657.1:p.Arg11Trp
ENST00000544180.6:c.31C>T	ENSP00000443787.1:p.Arg11Trp
NM_001163940.1:c.31C>T	NP_001157412.1:p.Arg11Trp
NM_002863.4:c.31C>T	NP_002854.3:p.Arg11Trp
NM_002863.5:c.31C>T MANE Select	NP_002854.3:p.Arg11Trp
NM_001163940.2:c.31C>T	NP_001157412.1:p.Arg11Trp