Canonical Allele Identifier: CA399811099

Gene: KIF18B

Linked Data

• MyVariant Identifiers: chr17:g.43003485G>T (hg19) ; chr17:g.44926117G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44926117G>T , CM000679.2:g.44926117G>T	GRCh38
NC_000017.10:g.43003485G>T , CM000679.1:g.43003485G>T	GRCh37
NC_000017.9:g.40359011G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000593135.6:c.2522C>A MANE Select	ENSP00000465992.1:p.Ala841Glu
ENST00000587309.5:c.*283C>A	ENSP00000465377.1:n.*283C>A
ENST00000593135.5:c.2522C>A	ENSP00000465992.1:p.Ala841Glu
NM_001264573.1:c.*283C>A	NP_001251503.1:n.*283C>A
NM_001265577.1:c.2522C>A	NP_001252506.1:p.Ala841Glu
XM_011524385.1:c.2585C>A	XP_011522687.1:p.Ala862Glu
XM_011524386.1:c.2558C>A	XP_011522688.1:p.Ala853Glu
XM_011524387.1:c.2558C>A	XP_011522689.1:p.Ala853Glu
XM_011524388.1:c.2549C>A	XP_011522690.1:p.Ala850Glu
XM_011524389.1:c.*283C>A	XP_011522691.1:n.*283C>A
XM_011524390.1:c.2480C>A	XP_011522692.1:p.Ala827Glu
XM_011524385.2:c.2585C>A	XP_011522687.1:p.Ala862Glu
XM_011524386.2:c.2558C>A	XP_011522688.1:p.Ala853Glu
XM_011524387.2:c.2558C>A	XP_011522689.1:p.Ala853Glu
XM_011524388.3:c.2549C>A	XP_011522690.1:p.Ala850Glu
XM_011524389.2:c.*283C>A	XP_011522691.1:n.*283C>A
XM_011524390.2:c.2480C>A	XP_011522692.1:p.Ala827Glu
NM_001264573.2:c.*283C>A	NP_001251503.1:n.*283C>A
NM_001265577.2:c.2522C>A MANE Select	NP_001252506.1:p.Ala841Glu