Canonical Allele Identifier: CA2136438552

Gene: PYGL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50944424C= , CM000676.2:g.50944424C=	GRCh38
NC_000014.8:g.51411142C= , CM000676.1:g.51411142C=	GRCh37
NC_000014.7:g.50480892C=	NCBI36
NG_012796.1:g.5107G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216392.8:c.-21G= MANE Select	ENSP00000216392.7:n.-21G=
ENST00000216392.7:c.-21G=	ENSP00000216392.7:n.-21G=
ENST00000530336.2:n.47G=
ENST00000532462.5:c.-21G=	ENSP00000431657.1:n.-21G=
ENST00000544180.6:c.-21G=	ENSP00000443787.1:n.-21G=
NM_001163940.1:c.-21G=	NP_001157412.1:n.-21G=
NM_002863.4:c.-21G=	NP_002854.3:n.-21G=
NM_002863.5:c.-21G= MANE Select	NP_002854.3:n.-21G=
NM_001163940.2:c.-21G=	NP_001157412.1:n.-21G=