Canonical Allele Identifier: CA399811129

Gene: KIF18B

Linked Data

• MyVariant Identifiers: chr17:g.43003494A>G (hg19) ; chr17:g.44926126A>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000593135.6:c.2513T>C MANE Select	ENSP00000465992.1:p.Val838Ala
ENST00000587309.5:c.*274T>C	ENSP00000465377.1:n.*274T>C
ENST00000593135.5:c.2513T>C	ENSP00000465992.1:p.Val838Ala
NM_001264573.1:c.*274T>C	NP_001251503.1:n.*274T>C
NM_001265577.1:c.2513T>C	NP_001252506.1:p.Val838Ala
XM_011524385.1:c.2576T>C	XP_011522687.1:p.Val859Ala
XM_011524386.1:c.2549T>C	XP_011522688.1:p.Val850Ala
XM_011524387.1:c.2549T>C	XP_011522689.1:p.Val850Ala
XM_011524388.1:c.2540T>C	XP_011522690.1:p.Val847Ala
XM_011524389.1:c.*274T>C	XP_011522691.1:n.*274T>C
XM_011524390.1:c.2471T>C	XP_011522692.1:p.Val824Ala
XM_011524385.2:c.2576T>C	XP_011522687.1:p.Val859Ala
XM_011524386.2:c.2549T>C	XP_011522688.1:p.Val850Ala
XM_011524387.2:c.2549T>C	XP_011522689.1:p.Val850Ala
XM_011524388.3:c.2540T>C	XP_011522690.1:p.Val847Ala
XM_011524389.2:c.*274T>C	XP_011522691.1:n.*274T>C
XM_011524390.2:c.2471T>C	XP_011522692.1:p.Val824Ala
NM_001264573.2:c.*274T>C	NP_001251503.1:n.*274T>C
NM_001265577.2:c.2513T>C MANE Select	NP_001252506.1:p.Val838Ala