Canonical Allele Identifier: CA2136438432

Gene: PYGL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50944193T= , CM000676.2:g.50944193T=	GRCh38
NC_000014.8:g.51410911T= , CM000676.1:g.51410911T=	GRCh37
NC_000014.7:g.50480661T=	NCBI36
NG_012796.1:g.5338A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216392.8:c.211A= MANE Select	ENSP00000216392.7:p.Thr71=
ENST00000216392.7:c.211A=	ENSP00000216392.7:p.Thr71=
ENST00000530336.2:n.278A=
ENST00000532462.5:c.211A=	ENSP00000431657.1:p.Thr71=
ENST00000544180.6:c.211A=	ENSP00000443787.1:p.Thr71=
NM_001163940.1:c.211A=	NP_001157412.1:p.Thr71=
NM_002863.4:c.211A=	NP_002854.3:p.Thr71=
NM_002863.5:c.211A= MANE Select	NP_002854.3:p.Thr71=
NM_001163940.2:c.211A=	NP_001157412.1:p.Thr71=