Canonical Allele Identifier: CA260818784

Gene: PYGL

Linked Data

• dbSNP Id: rs748619209
• MyVariant Identifiers: chr14:g.51372107A>G (hg19) ; chr14:g.50905389A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50905389A>G , CM000676.2:g.50905389A>G	GRCh38
NC_000014.8:g.51372107A>G , CM000676.1:g.51372107A>G	GRCh37
NC_000014.7:g.50441857A>G	NCBI36
NG_012796.1:g.44142T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216392.8:c.*3T>C MANE Select	ENSP00000216392.7:n.*3T>C
ENST00000216392.7:c.*3T>C	ENSP00000216392.7:n.*3T>C
ENST00000532462.5:c.2379+2882T>C	ENSP00000431657.1:n.2379+2882T>C
ENST00000544180.6:c.*3T>C	ENSP00000443787.1:n.*3T>C
NM_001163940.1:c.*3T>C	NP_001157412.1:n.*3T>C
NM_002863.4:c.*3T>C	NP_002854.3:n.*3T>C
NM_002863.5:c.*3T>C MANE Select	NP_002854.3:n.*3T>C
NM_001163940.2:c.*3T>C	NP_001157412.1:n.*3T>C