Canonical Allele Identifier: CA2136415062

Gene: PYGL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50910065A= , CM000676.2:g.50910065A=	GRCh38
NC_000014.8:g.51376783A= , CM000676.1:g.51376783A=	GRCh37
NC_000014.7:g.50446533A=	NCBI36
NG_012796.1:g.39466T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216392.8:c.2007T= MANE Select	ENSP00000216392.7:p.Thr669=
ENST00000216392.7:c.2007T=	ENSP00000216392.7:p.Thr669=
ENST00000532107.2:n.180T=
ENST00000532462.5:c.2007T=	ENSP00000431657.1:p.Thr669=
ENST00000544180.6:c.1905T=	ENSP00000443787.1:p.Thr635=
NM_001163940.1:c.1905T=	NP_001157412.1:p.Thr635=
NM_002863.4:c.2007T=	NP_002854.3:p.Thr669=
NM_002863.5:c.2007T= MANE Select	NP_002854.3:p.Thr669=
NM_001163940.2:c.1905T=	NP_001157412.1:p.Thr635=