Canonical Allele Identifier: CA389682649

Gene: PYGL

Linked Data

• MyVariant Identifiers: chr14:g.51376784G>T (hg19) ; chr14:g.50910066G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50910066G>T , CM000676.2:g.50910066G>T	GRCh38
NC_000014.8:g.51376784G>T , CM000676.1:g.51376784G>T	GRCh37
NC_000014.7:g.50446534G>T	NCBI36
NG_012796.1:g.39465C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000216392.8:c.2006C>A MANE Select	ENSP00000216392.7:p.Thr669Asn
ENST00000216392.7:c.2006C>A	ENSP00000216392.7:p.Thr669Asn
ENST00000532107.2:n.179C>A
ENST00000532462.5:c.2006C>A	ENSP00000431657.1:p.Thr669Asn
ENST00000544180.6:c.1904C>A	ENSP00000443787.1:p.Thr635Asn
NM_001163940.1:c.1904C>A	NP_001157412.1:p.Thr635Asn
NM_002863.4:c.2006C>A	NP_002854.3:p.Thr669Asn
NM_002863.5:c.2006C>A MANE Select	NP_002854.3:p.Thr669Asn
NM_001163940.2:c.1904C>A	NP_001157412.1:p.Thr635Asn