Canonical Allele Identifier: CA2136411272

Gene: PYGL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50905478C= , CM000676.2:g.50905478C=	GRCh38
NC_000014.8:g.51372196C= , CM000676.1:g.51372196C=	GRCh37
NC_000014.7:g.50441946C=	NCBI36
NG_012796.1:g.44053G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000216392.8:c.2458G= MANE Select	ENSP00000216392.7:p.Glu820=
ENST00000216392.7:c.2458G=	ENSP00000216392.7:p.Glu820=
ENST00000532462.5:c.2379+2793G=	ENSP00000431657.1:n.2379+2793G=
ENST00000544180.6:c.2356G=	ENSP00000443787.1:p.Glu786=
NM_001163940.1:c.2356G=	NP_001157412.1:p.Glu786=
NM_002863.4:c.2458G=	NP_002854.3:p.Glu820=
NM_002863.5:c.2458G= MANE Select	NP_002854.3:p.Glu820=
NM_001163940.2:c.2356G=	NP_001157412.1:p.Glu786=