Canonical Allele Identifier: CA1258629434
Gene: PLEK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.68371598C= , CM000664.2:g.68371598C= GRCh38
NC_000002.11:g.68598730C= , CM000664.1:g.68598730C= GRCh37
NC_000002.10:g.68452234C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000234313.8:c.42+6205C= MANE Select ENSP00000234313.7:n.42+6205C=
ENST00000234313.7:c.42+6205C= ENSP00000234313.7:n.42+6205C=
NM_002664.2:c.42+6205C= NP_002655.2:n.42+6205C=
XM_011532916.1:c.42+6205C= XP_011531218.1:n.42+6205C=
NM_002664.3:c.42+6205C= MANE Select NP_002655.2:n.42+6205C=