Canonical Allele Identifier: CA2136438448

Gene: PYGL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50944227C= , CM000676.2:g.50944227C=	GRCh38
NC_000014.8:g.51410945C= , CM000676.1:g.51410945C=	GRCh37
NC_000014.7:g.50480695C=	NCBI36
NG_012796.1:g.5304G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216392.8:c.177G= MANE Select	ENSP00000216392.7:p.Thr59=
ENST00000216392.7:c.177G=	ENSP00000216392.7:p.Thr59=
ENST00000530336.2:n.244G=
ENST00000532462.5:c.177G=	ENSP00000431657.1:p.Thr59=
ENST00000544180.6:c.177G=	ENSP00000443787.1:p.Thr59=
NM_001163940.1:c.177G=	NP_001157412.1:p.Thr59=
NM_002863.4:c.177G=	NP_002854.3:p.Thr59=
NM_002863.5:c.177G= MANE Select	NP_002854.3:p.Thr59=
NM_001163940.2:c.177G=	NP_001157412.1:p.Thr59=