Canonical Allele Identifier: CA1338005924

Gene: ILKAP

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238186708_238186710delinsGAA , CM000664.2:g.238186708_238186710delinsGAA	GRCh38
NC_000002.11:g.239095349_239095351delinsGAA , CM000664.1:g.239095349_239095351delinsGAA	GRCh37
NC_000002.10:g.238760088_238760090delinsGAA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000254654.8:c.425+1421_426-1421delinsTTC MANE Select	ENSP00000254654.3:n.425+1421_426-1421delinsTTC
ENST00000254654.7:c.425+1421_426-1421delinsTTC	ENSP00000254654.3:n.425+1421_426-1421delinsTTC
ENST00000457149.1:c.419+1421_420-1421delinsTTC	ENSP00000395301.1:n.419+1421_420-1421delinsTTC
ENST00000463129.5:n.973+1421_974-1421delinsTTC
ENST00000466468.5:n.348_350delinsTTC
ENST00000479400.1:n.464+1421_465-1421delinsTTC
ENST00000612675.4:c.425+1421_425+1423delinsTTC	ENSP00000477533.1:n.425+1421_425+1423delinsTTC
ENST00000622223.4:c.179-2597_179-2595delinsTTC	ENSP00000477542.1:n.179-2597_179-2595delinsTTC
NM_030768.2:c.425+1421_426-1421delinsTTC	NP_110395.1:n.425+1421_426-1421delinsTTC
XM_005246106.1:c.65+1421_66-1421delinsTTC	XP_005246163.1:n.65+1421_66-1421delinsTTC
XM_006712784.1:c.221+1421_222-1421delinsTTC	XP_006712847.1:n.221+1421_222-1421delinsTTC
XM_011511946.1:c.30-1423_30-1421delinsTTC	XP_011510248.1:n.30-1423_30-1421delinsTTC
XR_923033.1:n.574+1421_575-1421delinsTTC
XM_011511946.2:c.30-1423_30-1421delinsTTC	XP_011510248.1:n.30-1423_30-1421delinsTTC
XM_017005056.2:c.65+1421_66-1421delinsTTC	XP_016860545.1:n.65+1421_66-1421delinsTTC
XM_017005057.1:c.65+1421_66-1421delinsTTC	XP_016860546.1:n.65+1421_66-1421delinsTTC
XM_017005058.1:c.30-1423_30-1421delinsTTC	XP_016860547.1:n.30-1423_30-1421delinsTTC
XM_024453162.1:c.65+1421_66-1421delinsTTC	XP_024308930.1:n.65+1421_66-1421delinsTTC
NM_030768.3:c.425+1421_426-1421delinsTTC MANE Select	NP_110395.1:n.425+1421_426-1421delinsTTC