Canonical Allele Identifier: CA2196335

Gene: ILKAP

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.238194858T>C , CM000664.2:g.238194858T>C	GRCh38
NC_000002.11:g.239103499T>C , CM000664.1:g.239103499T>C	GRCh37
NC_000002.10:g.238768238T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_030768.3:c.68A>G MANE Select	NP_110395.1:p.Gln23Arg
ENST00000254654.8:c.68A>G MANE Select	ENSP00000254654.3:p.Gln23Arg
NM_030768.2:c.68A>G	NP_110395.1:p.Gln23Arg
ENST00000254654.7:c.68A>G	ENSP00000254654.3:p.Gln23Arg
ENST00000457149.1:c.68A>G	ENSP00000395301.1:p.Gln23Arg
ENST00000463129.5:n.153A>G
ENST00000467133.5:n.210A>G
ENST00000490837.1:n.210A>G
ENST00000498727.5:n.195A>G
ENST00000612675.4:c.68A>G	ENSP00000477533.1:p.Gln23Arg
ENST00000622223.4:c.68A>G	ENSP00000477542.1:p.Gln23Arg
XM_005246106.1:c.-306A>G	XP_005246163.1:n.-306A>G
XM_006712784.1:c.-160A>G	XP_006712847.1:n.-160A>G
XM_011511946.2:c.-192A>G	XP_011510248.1:n.-192A>G
XM_017005056.2:c.-283A>G	XP_016860545.1:n.-283A>G
XM_017005057.1:c.-654A>G	XP_016860546.1:n.-654A>G
XM_017005058.1:c.-215A>G	XP_016860547.1:n.-215A>G
XM_024453162.1:c.-2259A>G	XP_024308930.1:n.-2259A>G
XR_923033.1:n.217A>G