Canonical Allele Identifier: CA2261618630

Gene: KIF18B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44926109_44926132delinsCTGAGAGTGCTCTCCCCACCCTGA , CM000679.2:g.44926109_44926132delinsCTGAGAGTGCTCTCCCCACCCTGA	GRCh38
NC_000017.10:g.43003477_43003500delinsCTGAGAGTGCTCTCCCCACCCTGA , CM000679.1:g.43003477_43003500delinsCTGAGAGTGCTCTCCCCACCCTGA	GRCh37
NC_000017.9:g.40359003_40359026delinsCTGAGAGTGCTCTCCCCACCCTGA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000593135.6:c.2507_2530delinsTCAGGGTGGGGAGAGCACTCTCAG MANE Select	ENSP00000465992.1:p.Ile836=
ENST00000587309.5:c.*268_*291delinsTCAGGGTGGGGAGAGCACTCTCAG	ENSP00000465377.1:n.*268_*291delinsTCAGGGTGGGGAGAGCACTCTCAG
ENST00000593135.5:c.2507_2530delinsTCAGGGTGGGGAGAGCACTCTCAG	ENSP00000465992.1:p.Ile836=
NM_001264573.1:c.*268_*291delinsTCAGGGTGGGGAGAGCACTCTCAG	NP_001251503.1:n.*268_*291delinsTCAGGGTGGGGAGAGCACTCTCAG
NM_001265577.1:c.2507_2530delinsTCAGGGTGGGGAGAGCACTCTCAG	NP_001252506.1:p.Ile836=
XM_011524385.1:c.2570_2593delinsTCAGGGTGGGGAGAGCACTCTCAG	XP_011522687.1:p.Ile857=
XM_011524386.1:c.2543_2566delinsTCAGGGTGGGGAGAGCACTCTCAG	XP_011522688.1:p.Ile848=
XM_011524387.1:c.2543_2566delinsTCAGGGTGGGGAGAGCACTCTCAG	XP_011522689.1:p.Ile848=
XM_011524388.1:c.2534_2557delinsTCAGGGTGGGGAGAGCACTCTCAG	XP_011522690.1:p.Ile845=
XM_011524389.1:c.*268_*291delinsTCAGGGTGGGGAGAGCACTCTCAG	XP_011522691.1:n.*268_*291delinsTCAGGGTGGGGAGAGCACTCTCAG
XM_011524390.1:c.2465_2488delinsTCAGGGTGGGGAGAGCACTCTCAG	XP_011522692.1:p.Ile822=
XM_011524385.2:c.2570_2593delinsTCAGGGTGGGGAGAGCACTCTCAG	XP_011522687.1:p.Ile857=
XM_011524386.2:c.2543_2566delinsTCAGGGTGGGGAGAGCACTCTCAG	XP_011522688.1:p.Ile848=
XM_011524387.2:c.2543_2566delinsTCAGGGTGGGGAGAGCACTCTCAG	XP_011522689.1:p.Ile848=
XM_011524388.3:c.2534_2557delinsTCAGGGTGGGGAGAGCACTCTCAG	XP_011522690.1:p.Ile845=
XM_011524389.2:c.*268_*291delinsTCAGGGTGGGGAGAGCACTCTCAG	XP_011522691.1:n.*268_*291delinsTCAGGGTGGGGAGAGCACTCTCAG
XM_011524390.2:c.2465_2488delinsTCAGGGTGGGGAGAGCACTCTCAG	XP_011522692.1:p.Ile822=
NM_001264573.2:c.*268_*291delinsTCAGGGTGGGGAGAGCACTCTCAG	NP_001251503.1:n.*268_*291delinsTCAGGGTGGGGAGAGCACTCTCAG
NM_001265577.2:c.2507_2530delinsTCAGGGTGGGGAGAGCACTCTCAG MANE Select	NP_001252506.1:p.Ile836=