Canonical Allele Identifier: CA2663869689

Gene: ILKAP

Linked Data

• gnomAD v4: 2-238186685-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238186685G>C , CM000664.2:g.238186685G>C	GRCh38
NC_000002.11:g.239095326G>C , CM000664.1:g.239095326G>C	GRCh37
NC_000002.10:g.238760065G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254654.8:c.426-1398C>G MANE Select	ENSP00000254654.3:n.426-1398C>G
ENST00000254654.7:c.426-1398C>G	ENSP00000254654.3:n.426-1398C>G
ENST00000457149.1:c.420-1398C>G	ENSP00000395301.1:n.420-1398C>G
ENST00000463129.5:n.974-1398C>G
ENST00000466468.5:n.373C>G
ENST00000479400.1:n.465-1398C>G
ENST00000612675.4:c.425+1446C>G	ENSP00000477533.1:n.425+1446C>G
ENST00000622223.4:c.179-2572C>G	ENSP00000477542.1:n.179-2572C>G
NM_030768.2:c.426-1398C>G	NP_110395.1:n.426-1398C>G
XM_005246106.1:c.66-1398C>G	XP_005246163.1:n.66-1398C>G
XM_006712784.1:c.222-1398C>G	XP_006712847.1:n.222-1398C>G
XM_011511946.1:c.30-1398C>G	XP_011510248.1:n.30-1398C>G
XR_923033.1:n.575-1398C>G
XM_011511946.2:c.30-1398C>G	XP_011510248.1:n.30-1398C>G
XM_017005056.2:c.66-1398C>G	XP_016860545.1:n.66-1398C>G
XM_017005057.1:c.66-1398C>G	XP_016860546.1:n.66-1398C>G
XM_017005058.1:c.30-1398C>G	XP_016860547.1:n.30-1398C>G
XM_024453162.1:c.66-1398C>G	XP_024308930.1:n.66-1398C>G
NM_030768.3:c.426-1398C>G MANE Select	NP_110395.1:n.426-1398C>G