Canonical Allele Identifier: CA389682736
Gene: PYGL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50910091T>G , CM000676.2:g.50910091T>G GRCh38
NC_000014.8:g.51376809T>G , CM000676.1:g.51376809T>G GRCh37
NC_000014.7:g.50446559T>G NCBI36
NG_012796.1:g.39440A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000216392.8:c.1981A>C MANE Select ENSP00000216392.7:p.Thr661Pro
ENST00000216392.7:c.1981A>C ENSP00000216392.7:p.Thr661Pro
ENST00000532107.2:n.154A>C
ENST00000532462.5:c.1981A>C ENSP00000431657.1:p.Thr661Pro
ENST00000544180.6:c.1879A>C ENSP00000443787.1:p.Thr627Pro
NM_001163940.1:c.1879A>C NP_001157412.1:p.Thr627Pro
NM_002863.4:c.1981A>C NP_002854.3:p.Thr661Pro
NM_002863.5:c.1981A>C MANE Select NP_002854.3:p.Thr661Pro
NM_001163940.2:c.1879A>C NP_001157412.1:p.Thr627Pro