Canonical Allele Identifier: CA2136438437

Gene: PYGL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50944204C= , CM000676.2:g.50944204C=	GRCh38
NC_000014.8:g.51410922C= , CM000676.1:g.51410922C=	GRCh37
NC_000014.7:g.50480672C=	NCBI36
NG_012796.1:g.5327G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216392.8:c.200G= MANE Select	ENSP00000216392.7:p.Arg67=
ENST00000216392.7:c.200G=	ENSP00000216392.7:p.Arg67=
ENST00000530336.2:n.267G=
ENST00000532462.5:c.200G=	ENSP00000431657.1:p.Arg67=
ENST00000544180.6:c.200G=	ENSP00000443787.1:p.Arg67=
NM_001163940.1:c.200G=	NP_001157412.1:p.Arg67=
NM_002863.4:c.200G=	NP_002854.3:p.Arg67=
NM_002863.5:c.200G= MANE Select	NP_002854.3:p.Arg67=
NM_001163940.2:c.200G=	NP_001157412.1:p.Arg67=