Canonical Allele Identifier: CA1258629390
Gene: PLEK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.68371468T= , CM000664.2:g.68371468T= GRCh38
NC_000002.11:g.68598600T= , CM000664.1:g.68598600T= GRCh37
NC_000002.10:g.68452104T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000234313.8:c.42+6075T= MANE Select ENSP00000234313.7:n.42+6075T=
ENST00000234313.7:c.42+6075T= ENSP00000234313.7:n.42+6075T=
NM_002664.2:c.42+6075T= NP_002655.2:n.42+6075T=
XM_011532916.1:c.42+6075T= XP_011531218.1:n.42+6075T=
NM_002664.3:c.42+6075T= MANE Select NP_002655.2:n.42+6075T=