Canonical Allele Identifier: CA2136416351

Gene: PYGL

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50911674C= , CM000676.2:g.50911674C=	GRCh38
NC_000014.8:g.51378392C= , CM000676.1:g.51378392C=	GRCh37
NC_000014.7:g.50448142C=	NCBI36
NG_012796.1:g.37857G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216392.8:c.1969+56G= MANE Select	ENSP00000216392.7:n.1969+56G=
ENST00000216392.7:c.1969+56G=	ENSP00000216392.7:n.1969+56G=
ENST00000532107.2:n.142+56G=
ENST00000532462.5:c.1969+56G=	ENSP00000431657.1:n.1969+56G=
ENST00000544180.6:c.1867+56G=	ENSP00000443787.1:n.1867+56G=
NM_001163940.1:c.1867+56G=	NP_001157412.1:n.1867+56G=
NM_002863.4:c.1969+56G=	NP_002854.3:n.1969+56G=
NM_002863.5:c.1969+56G= MANE Select	NP_002854.3:n.1969+56G=
NM_001163940.2:c.1867+56G=	NP_001157412.1:n.1867+56G=