Canonical Allele Identifier: CA2663869684

Gene: ILKAP

Linked Data

• gnomAD v4: 2-238186681-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238186681A>T , CM000664.2:g.238186681A>T	GRCh38
NC_000002.11:g.239095322A>T , CM000664.1:g.239095322A>T	GRCh37
NC_000002.10:g.238760061A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254654.8:c.426-1394T>A MANE Select	ENSP00000254654.3:n.426-1394T>A
ENST00000254654.7:c.426-1394T>A	ENSP00000254654.3:n.426-1394T>A
ENST00000457149.1:c.420-1394T>A	ENSP00000395301.1:n.420-1394T>A
ENST00000463129.5:n.974-1394T>A
ENST00000466468.5:n.377T>A
ENST00000479400.1:n.465-1394T>A
ENST00000612675.4:c.425+1450T>A	ENSP00000477533.1:n.425+1450T>A
ENST00000622223.4:c.179-2568T>A	ENSP00000477542.1:n.179-2568T>A
NM_030768.2:c.426-1394T>A	NP_110395.1:n.426-1394T>A
XM_005246106.1:c.66-1394T>A	XP_005246163.1:n.66-1394T>A
XM_006712784.1:c.222-1394T>A	XP_006712847.1:n.222-1394T>A
XM_011511946.1:c.30-1394T>A	XP_011510248.1:n.30-1394T>A
XR_923033.1:n.575-1394T>A
XM_011511946.2:c.30-1394T>A	XP_011510248.1:n.30-1394T>A
XM_017005056.2:c.66-1394T>A	XP_016860545.1:n.66-1394T>A
XM_017005057.1:c.66-1394T>A	XP_016860546.1:n.66-1394T>A
XM_017005058.1:c.30-1394T>A	XP_016860547.1:n.30-1394T>A
XM_024453162.1:c.66-1394T>A	XP_024308930.1:n.66-1394T>A
NM_030768.3:c.426-1394T>A MANE Select	NP_110395.1:n.426-1394T>A