Canonical Allele Identifier: CA2136438549

Gene: PYGL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50944416G= , CM000676.2:g.50944416G=	GRCh38
NC_000014.8:g.51411134G= , CM000676.1:g.51411134G=	GRCh37
NC_000014.7:g.50480884G=	NCBI36
NG_012796.1:g.5115C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216392.8:c.-13C= MANE Select	ENSP00000216392.7:n.-13C=
ENST00000216392.7:c.-13C=	ENSP00000216392.7:n.-13C=
ENST00000530336.2:n.55C=
ENST00000532462.5:c.-13C=	ENSP00000431657.1:n.-13C=
ENST00000544180.6:c.-13C=	ENSP00000443787.1:n.-13C=
NM_001163940.1:c.-13C=	NP_001157412.1:n.-13C=
NM_002863.4:c.-13C=	NP_002854.3:n.-13C=
NM_002863.5:c.-13C= MANE Select	NP_002854.3:n.-13C=
NM_001163940.2:c.-13C=	NP_001157412.1:n.-13C=