Canonical Allele Identifier: CA2136419313

Gene: PYGL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50915785T= , CM000676.2:g.50915785T=	GRCh38
NC_000014.8:g.51382503T= , CM000676.1:g.51382503T=	GRCh37
NC_000014.7:g.50452253T=	NCBI36
NG_012796.1:g.33746A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000216392.8:c.1239+40A= MANE Select	ENSP00000216392.7:n.1239+40A=
ENST00000216392.7:c.1239+40A=	ENSP00000216392.7:n.1239+40A=
ENST00000528757.2:n.116+40A=
ENST00000532462.5:c.1239+40A=	ENSP00000431657.1:n.1239+40A=
ENST00000544180.6:c.1137+40A=	ENSP00000443787.1:n.1137+40A=
NM_001163940.1:c.1137+40A=	NP_001157412.1:n.1137+40A=
NM_002863.4:c.1239+40A=	NP_002854.3:n.1239+40A=
NM_002863.5:c.1239+40A= MANE Select	NP_002854.3:n.1239+40A=
NM_001163940.2:c.1137+40A=	NP_001157412.1:n.1137+40A=