Canonical Allele Identifier: CA389682402
Gene: PYGL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50909997G>T , CM000676.2:g.50909997G>T GRCh38
NC_000014.8:g.51376715G>T , CM000676.1:g.51376715G>T GRCh37
NC_000014.7:g.50446465G>T NCBI36
NG_012796.1:g.39534C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000216392.8:c.2075C>A MANE Select ENSP00000216392.7:p.Thr692Asn
ENST00000216392.7:c.2075C>A ENSP00000216392.7:p.Thr692Asn
ENST00000532107.2:n.248C>A
ENST00000532462.5:c.2075C>A ENSP00000431657.1:p.Thr692Asn
ENST00000544180.6:c.1973C>A ENSP00000443787.1:p.Thr658Asn
NM_001163940.1:c.1973C>A NP_001157412.1:p.Thr658Asn
NM_002863.4:c.2075C>A NP_002854.3:p.Thr692Asn
NM_002863.5:c.2075C>A MANE Select NP_002854.3:p.Thr692Asn
NM_001163940.2:c.1973C>A NP_001157412.1:p.Thr658Asn