Canonical Allele Identifier: CA2261618642

Gene: KIF18B

Linked Data

• dbSNP Id: rs2052019901

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44926129dup , CM000679.2:g.44926129dup	GRCh38
NC_000017.10:g.43003497dup , CM000679.1:g.43003497dup	GRCh37
NC_000017.9:g.40359023dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593135.6:c.2512dup MANE Select	ENSP00000465992.1:p.Val838GlyfsTer22
ENST00000587309.5:c.*273dup	ENSP00000465377.1:n.*273dup
ENST00000593135.5:c.2512dup	ENSP00000465992.1:p.Val838GlyfsTer22
NM_001264573.1:c.*273dup	NP_001251503.1:n.*273dup
NM_001265577.1:c.2512dup	NP_001252506.1:p.Val838GlyfsTer22
XM_011524385.1:c.2575dup	XP_011522687.1:p.Val859GlyfsTer22
XM_011524386.1:c.2548dup	XP_011522688.1:p.Val850GlyfsTer22
XM_011524387.1:c.2548dup	XP_011522689.1:p.Val850GlyfsTer22
XM_011524388.1:c.2539dup	XP_011522690.1:p.Val847GlyfsTer22
XM_011524389.1:c.*273dup	XP_011522691.1:n.*273dup
XM_011524390.1:c.2470dup	XP_011522692.1:p.Val824GlyfsTer22
XM_011524385.2:c.2575dup	XP_011522687.1:p.Val859GlyfsTer22
XM_011524386.2:c.2548dup	XP_011522688.1:p.Val850GlyfsTer22
XM_011524387.2:c.2548dup	XP_011522689.1:p.Val850GlyfsTer22
XM_011524388.3:c.2539dup	XP_011522690.1:p.Val847GlyfsTer22
XM_011524389.2:c.*273dup	XP_011522691.1:n.*273dup
XM_011524390.2:c.2470dup	XP_011522692.1:p.Val824GlyfsTer22
NM_001264573.2:c.*273dup	NP_001251503.1:n.*273dup
NM_001265577.2:c.2512dup MANE Select	NP_001252506.1:p.Val838GlyfsTer22