Canonical Allele Identifier: CA389682366
Gene: PYGL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50909988C>A , CM000676.2:g.50909988C>A GRCh38
NC_000014.8:g.51376706C>A , CM000676.1:g.51376706C>A GRCh37
NC_000014.7:g.50446456C>A NCBI36
NG_012796.1:g.39543G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000216392.8:c.2084G>T MANE Select ENSP00000216392.7:p.Gly695Val
ENST00000216392.7:c.2084G>T ENSP00000216392.7:p.Gly695Val
ENST00000532107.2:n.257G>T
ENST00000532462.5:c.2084G>T ENSP00000431657.1:p.Gly695Val
ENST00000544180.6:c.1982G>T ENSP00000443787.1:p.Gly661Val
NM_001163940.1:c.1982G>T NP_001157412.1:p.Gly661Val
NM_002863.4:c.2084G>T NP_002854.3:p.Gly695Val
NM_002863.5:c.2084G>T MANE Select NP_002854.3:p.Gly695Val
NM_001163940.2:c.1982G>T NP_001157412.1:p.Gly661Val