Canonical Allele Identifier: CA399811105

Gene: KIF18B

Linked Data

• MyVariant Identifiers: chr17:g.43003486C>T (hg19) ; chr17:g.44926118C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44926118C>T , CM000679.2:g.44926118C>T	GRCh38
NC_000017.10:g.43003486C>T , CM000679.1:g.43003486C>T	GRCh37
NC_000017.9:g.40359012C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593135.6:c.2521G>A MANE Select	ENSP00000465992.1:p.Ala841Thr
ENST00000587309.5:c.*282G>A	ENSP00000465377.1:n.*282G>A
ENST00000593135.5:c.2521G>A	ENSP00000465992.1:p.Ala841Thr
NM_001264573.1:c.*282G>A	NP_001251503.1:n.*282G>A
NM_001265577.1:c.2521G>A	NP_001252506.1:p.Ala841Thr
XM_011524385.1:c.2584G>A	XP_011522687.1:p.Ala862Thr
XM_011524386.1:c.2557G>A	XP_011522688.1:p.Ala853Thr
XM_011524387.1:c.2557G>A	XP_011522689.1:p.Ala853Thr
XM_011524388.1:c.2548G>A	XP_011522690.1:p.Ala850Thr
XM_011524389.1:c.*282G>A	XP_011522691.1:n.*282G>A
XM_011524390.1:c.2479G>A	XP_011522692.1:p.Ala827Thr
XM_011524385.2:c.2584G>A	XP_011522687.1:p.Ala862Thr
XM_011524386.2:c.2557G>A	XP_011522688.1:p.Ala853Thr
XM_011524387.2:c.2557G>A	XP_011522689.1:p.Ala853Thr
XM_011524388.3:c.2548G>A	XP_011522690.1:p.Ala850Thr
XM_011524389.2:c.*282G>A	XP_011522691.1:n.*282G>A
XM_011524390.2:c.2479G>A	XP_011522692.1:p.Ala827Thr
NM_001264573.2:c.*282G>A	NP_001251503.1:n.*282G>A
NM_001265577.2:c.2521G>A MANE Select	NP_001252506.1:p.Ala841Thr