Canonical Allele Identifier: CA2136438513

Gene: PYGL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50944366T= , CM000676.2:g.50944366T=	GRCh38
NC_000014.8:g.51411084T= , CM000676.1:g.51411084T=	GRCh37
NC_000014.7:g.50480834T=	NCBI36
NG_012796.1:g.5165A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000216392.8:c.38A= MANE Select	ENSP00000216392.7:p.Gln13=
ENST00000216392.7:c.38A=	ENSP00000216392.7:p.Gln13=
ENST00000530336.2:n.105A=
ENST00000532462.5:c.38A=	ENSP00000431657.1:p.Gln13=
ENST00000544180.6:c.38A=	ENSP00000443787.1:p.Gln13=
NM_001163940.1:c.38A=	NP_001157412.1:p.Gln13=
NM_002863.4:c.38A=	NP_002854.3:p.Gln13=
NM_002863.5:c.38A= MANE Select	NP_002854.3:p.Gln13=
NM_001163940.2:c.38A=	NP_001157412.1:p.Gln13=