Canonical Allele Identifier: CA1043871413
Gene: ILKAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238186710_238186720dup , CM000664.2:g.238186710_238186720dup GRCh38
NC_000002.11:g.239095351_239095361dup , CM000664.1:g.239095351_239095361dup GRCh37
NC_000002.10:g.238760090_238760100dup NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000254654.8:c.425+1412_426-1422dup MANE Select ENSP00000254654.3:n.425+1412_426-1422dup
ENST00000254654.7:c.425+1412_426-1422dup ENSP00000254654.3:n.425+1412_426-1422dup
ENST00000457149.1:c.419+1412_420-1422dup ENSP00000395301.1:n.419+1412_420-1422dup
ENST00000463129.5:n.973+1412_974-1422dup
ENST00000466468.5:n.339_349dup
ENST00000479400.1:n.464+1412_465-1422dup
ENST00000612675.4:c.425+1412_425+1422dup ENSP00000477533.1:n.425+1412_425+1422dup
ENST00000622223.4:c.179-2606_179-2596dup ENSP00000477542.1:n.179-2606_179-2596dup
NM_030768.2:c.425+1412_426-1422dup NP_110395.1:n.425+1412_426-1422dup
XM_005246106.1:c.65+1412_66-1422dup XP_005246163.1:n.65+1412_66-1422dup
XM_006712784.1:c.221+1412_222-1422dup XP_006712847.1:n.221+1412_222-1422dup
XM_011511946.1:c.30-1432_30-1422dup XP_011510248.1:n.30-1432_30-1422dup
XR_923033.1:n.574+1412_575-1422dup
XM_011511946.2:c.30-1432_30-1422dup XP_011510248.1:n.30-1432_30-1422dup
XM_017005056.2:c.65+1412_66-1422dup XP_016860545.1:n.65+1412_66-1422dup
XM_017005057.1:c.65+1412_66-1422dup XP_016860546.1:n.65+1412_66-1422dup
XM_017005058.1:c.30-1432_30-1422dup XP_016860547.1:n.30-1432_30-1422dup
XM_024453162.1:c.65+1412_66-1422dup XP_024308930.1:n.65+1412_66-1422dup
NM_030768.3:c.425+1412_426-1422dup MANE Select NP_110395.1:n.425+1412_426-1422dup