Canonical Allele Identifier: CA486371950

Gene: PYGL

Linked Data

• MyVariant Identifiers: chr14:g.51372111C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50905393C>T , CM000676.2:g.50905393C>T	GRCh38
NC_000014.8:g.51372111C>T , CM000676.1:g.51372111C>T	GRCh37
NC_000014.7:g.50441861C>T	NCBI36
NG_012796.1:g.44138G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216392.8:c.2543G>A MANE Select	ENSP00000216392.7:p.Ter848=
ENST00000216392.7:c.2543G>A	ENSP00000216392.7:p.Ter848=
ENST00000532462.5:c.2379+2878G>A	ENSP00000431657.1:n.2379+2878G>A
ENST00000544180.6:c.2441G>A	ENSP00000443787.1:p.Ter814=
NM_001163940.1:c.2441G>A	NP_001157412.1:p.Ter814=
NM_002863.4:c.2543G>A	NP_002854.3:p.Ter848=
NM_002863.5:c.2543G>A MANE Select	NP_002854.3:p.Ter848=
NM_001163940.2:c.2441G>A	NP_001157412.1:p.Ter814=