Canonical Allele Identifier: CA1258629582
Gene: PLEK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.68371918T= , CM000664.2:g.68371918T= GRCh38
NC_000002.11:g.68599050T= , CM000664.1:g.68599050T= GRCh37
NC_000002.10:g.68452554T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000234313.8:c.42+6525T= MANE Select ENSP00000234313.7:n.42+6525T=
ENST00000234313.7:c.42+6525T= ENSP00000234313.7:n.42+6525T=
NM_002664.2:c.42+6525T= NP_002655.2:n.42+6525T=
XM_011532916.1:c.42+6525T= XP_011531218.1:n.42+6525T=
NM_002664.3:c.42+6525T= MANE Select NP_002655.2:n.42+6525T=
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