Canonical Allele Identifier: CA2136411069

Gene: PYGL

Linked Data

• dbSNP Id: rs2050319699

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50905326C>A , CM000676.2:g.50905326C>A	GRCh38
NC_000014.8:g.51372044C>A , CM000676.1:g.51372044C>A	GRCh37
NC_000014.7:g.50441794C>A	NCBI36
NG_012796.1:g.44205G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216392.8:c.*66G>T MANE Select	ENSP00000216392.7:n.*66G>T
ENST00000216392.7:c.*66G>T	ENSP00000216392.7:n.*66G>T
ENST00000532462.5:c.2379+2945G>T	ENSP00000431657.1:n.2379+2945G>T
ENST00000544180.6:c.*66G>T	ENSP00000443787.1:n.*66G>T
NM_001163940.1:c.*66G>T	NP_001157412.1:n.*66G>T
NM_002863.4:c.*66G>T	NP_002854.3:n.*66G>T
NM_002863.5:c.*66G>T MANE Select	NP_002854.3:n.*66G>T
NM_001163940.2:c.*66G>T	NP_001157412.1:n.*66G>T