Canonical Allele Identifier: CA2261618641

Gene: KIF18B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44926126A= , CM000679.2:g.44926126A=	GRCh38
NC_000017.10:g.43003494A= , CM000679.1:g.43003494A=	GRCh37
NC_000017.9:g.40359020A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593135.6:c.2513T= MANE Select	ENSP00000465992.1:p.Val838=
ENST00000587309.5:c.*274T=	ENSP00000465377.1:n.*274T=
ENST00000593135.5:c.2513T=	ENSP00000465992.1:p.Val838=
NM_001264573.1:c.*274T=	NP_001251503.1:n.*274T=
NM_001265577.1:c.2513T=	NP_001252506.1:p.Val838=
XM_011524385.1:c.2576T=	XP_011522687.1:p.Val859=
XM_011524386.1:c.2549T=	XP_011522688.1:p.Val850=
XM_011524387.1:c.2549T=	XP_011522689.1:p.Val850=
XM_011524388.1:c.2540T=	XP_011522690.1:p.Val847=
XM_011524389.1:c.*274T=	XP_011522691.1:n.*274T=
XM_011524390.1:c.2471T=	XP_011522692.1:p.Val824=
XM_011524385.2:c.2576T=	XP_011522687.1:p.Val859=
XM_011524386.2:c.2549T=	XP_011522688.1:p.Val850=
XM_011524387.2:c.2549T=	XP_011522689.1:p.Val850=
XM_011524388.3:c.2540T=	XP_011522690.1:p.Val847=
XM_011524389.2:c.*274T=	XP_011522691.1:n.*274T=
XM_011524390.2:c.2471T=	XP_011522692.1:p.Val824=
NM_001264573.2:c.*274T=	NP_001251503.1:n.*274T=
NM_001265577.2:c.2513T= MANE Select	NP_001252506.1:p.Val838=