Canonical Allele Identifier: CA389682698
Gene: PYGL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50910079C>T , CM000676.2:g.50910079C>T GRCh38
NC_000014.8:g.51376797C>T , CM000676.1:g.51376797C>T GRCh37
NC_000014.7:g.50446547C>T NCBI36
NG_012796.1:g.39452G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000216392.8:c.1993G>A MANE Select ENSP00000216392.7:p.Glu665Lys
ENST00000216392.7:c.1993G>A ENSP00000216392.7:p.Glu665Lys
ENST00000532107.2:n.166G>A
ENST00000532462.5:c.1993G>A ENSP00000431657.1:p.Glu665Lys
ENST00000544180.6:c.1891G>A ENSP00000443787.1:p.Glu631Lys
NM_001163940.1:c.1891G>A NP_001157412.1:p.Glu631Lys
NM_002863.4:c.1993G>A NP_002854.3:p.Glu665Lys
NM_002863.5:c.1993G>A MANE Select NP_002854.3:p.Glu665Lys
NM_001163940.2:c.1891G>A NP_001157412.1:p.Glu631Lys