Canonical Allele Identifier: CA486372869

Gene: PYGL

Linked Data

• MyVariant Identifiers: chr14:g.51372263G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50905545G>C , CM000676.2:g.50905545G>C	GRCh38
NC_000014.8:g.51372263G>C , CM000676.1:g.51372263G>C	GRCh37
NC_000014.7:g.50442013G>C	NCBI36
NG_012796.1:g.43986C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216392.8:c.2391C>G MANE Select	ENSP00000216392.7:p.Ala797=
ENST00000216392.7:c.2391C>G	ENSP00000216392.7:p.Ala797=
ENST00000532462.5:c.2379+2726C>G	ENSP00000431657.1:n.2379+2726C>G
ENST00000544180.6:c.2289C>G	ENSP00000443787.1:p.Ala763=
NM_001163940.1:c.2289C>G	NP_001157412.1:p.Ala763=
NM_002863.4:c.2391C>G	NP_002854.3:p.Ala797=
NM_002863.5:c.2391C>G MANE Select	NP_002854.3:p.Ala797=
NM_001163940.2:c.2289C>G	NP_001157412.1:p.Ala763=