Canonical Allele Identifier: CA2261621325

Gene: KIF18B

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44932518G>T , CM000679.2:g.44932518G>T	GRCh38
NC_000017.10:g.43009886G>T , CM000679.1:g.43009886G>T	GRCh37
NC_000017.9:g.40365412G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593135.6:c.1238+155C>A MANE Select	ENSP00000465992.1:n.1238+155C>A
ENST00000585687.1:n.385C>A
ENST00000587309.5:c.1238+155C>A	ENSP00000465377.1:n.1238+155C>A
ENST00000590129.1:c.1265+155C>A	ENSP00000465501.1:n.1265+155C>A
ENST00000593135.5:c.1238+155C>A	ENSP00000465992.1:n.1238+155C>A
NM_001264573.1:c.1238+155C>A	NP_001251503.1:n.1238+155C>A
NM_001265577.1:c.1238+155C>A	NP_001252506.1:n.1238+155C>A
XM_011524385.1:c.1265+155C>A	XP_011522687.1:n.1265+155C>A
XM_011524386.1:c.1238+155C>A	XP_011522688.1:n.1238+155C>A
XM_011524387.1:c.1265+155C>A	XP_011522689.1:n.1265+155C>A
XM_011524388.1:c.1265+155C>A	XP_011522690.1:n.1265+155C>A
XM_011524389.1:c.1265+155C>A	XP_011522691.1:n.1265+155C>A
XM_011524390.1:c.1160+155C>A	XP_011522692.1:n.1160+155C>A
XM_011524391.1:c.1304C>A	XP_011522693.1:p.Thr435Asn
XM_011524385.2:c.1265+155C>A	XP_011522687.1:n.1265+155C>A
XM_011524386.2:c.1238+155C>A	XP_011522688.1:n.1238+155C>A
XM_011524387.2:c.1265+155C>A	XP_011522689.1:n.1265+155C>A
XM_011524388.3:c.1265+155C>A	XP_011522690.1:n.1265+155C>A
XM_011524389.2:c.1265+155C>A	XP_011522691.1:n.1265+155C>A
XM_011524390.2:c.1160+155C>A	XP_011522692.1:n.1160+155C>A
XM_011524391.3:c.1304C>A	XP_011522693.1:p.Thr435Asn
NM_001264573.2:c.1238+155C>A	NP_001251503.1:n.1238+155C>A
NM_001265577.2:c.1238+155C>A MANE Select	NP_001252506.1:n.1238+155C>A