Canonical Allele Identifier: CA2136438592

Gene: PYGL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50944468G= , CM000676.2:g.50944468G=	GRCh38
NC_000014.8:g.51411186G= , CM000676.1:g.51411186G=	GRCh37
NC_000014.7:g.50480936G=	NCBI36
NG_012796.1:g.5063C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216392.8:c.-65C= MANE Select	ENSP00000216392.7:n.-65C=
ENST00000216392.7:c.-65C=	ENSP00000216392.7:n.-65C=
ENST00000530336.2:n.3C=
ENST00000544180.6:c.-65C=	ENSP00000443787.1:n.-65C=
NM_001163940.1:c.-65C=	NP_001157412.1:n.-65C=
NM_002863.4:c.-65C=	NP_002854.3:n.-65C=
NM_002863.5:c.-65C= MANE Select	NP_002854.3:n.-65C=
NM_001163940.2:c.-65C=	NP_001157412.1:n.-65C=