Canonical Allele Identifier: CA486383294
Gene: PYGL HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.51382600C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50915882C>T , CM000676.2:g.50915882C>T GRCh38
NC_000014.8:g.51382600C>T , CM000676.1:g.51382600C>T GRCh37
NC_000014.7:g.50452350C>T NCBI36
NG_012796.1:g.33649G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000216392.8:c.1182G>A MANE Select ENSP00000216392.7:p.Glu394=
ENST00000216392.7:c.1182G>A ENSP00000216392.7:p.Glu394=
ENST00000528757.2:n.59G>A
ENST00000532462.5:c.1182G>A ENSP00000431657.1:p.Glu394=
ENST00000544180.6:c.1080G>A ENSP00000443787.1:p.Glu360=
NM_001163940.1:c.1080G>A NP_001157412.1:p.Glu360=
NM_002863.4:c.1182G>A NP_002854.3:p.Glu394=
NM_002863.5:c.1182G>A MANE Select NP_002854.3:p.Glu394=
NM_001163940.2:c.1080G>A NP_001157412.1:p.Glu360=