Canonical Allele Identifier: CA1773607346

Gene: KIF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.29137505A= , CM000670.2:g.29137505A=	GRCh38
NC_000008.10:g.28995022A= , CM000670.1:g.28995022A=	GRCh37
NC_000008.9:g.29050941A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_015254.4:c.2613+2558T= MANE Select	NP_056069.2:n.2613+2558T=
ENST00000524189.6:c.2613+2558T= MANE Select	ENSP00000427900.1:n.2613+2558T=
NM_015254.3:c.2613+2558T=	NP_056069.2:n.2613+2558T=
ENST00000524189.5:c.2613+2558T=	ENSP00000427900.1:n.2613+2558T=
XM_005273458.1:c.2613+2558T=	XP_005273515.1:n.2613+2558T=
XM_011544457.1:c.2613+2558T=	XP_011542759.1:n.2613+2558T=
XM_011544458.1:c.2613+2558T=	XP_011542760.1:n.2613+2558T=
XM_011544459.1:c.2421+2558T=	XP_011542761.1:n.2421+2558T=
XM_011544459.3:c.2421+2558T=	XP_011542761.1:n.2421+2558T=
XM_011544460.1:c.2421+2558T=	XP_011542762.1:n.2421+2558T=
XM_011544460.3:c.2421+2558T=	XP_011542762.1:n.2421+2558T=
XM_011544461.1:c.2421+2558T=	XP_011542763.1:n.2421+2558T=
XM_017013257.1:c.2613+2558T=	XP_016868746.1:n.2613+2558T=
XR_949621.1:n.93-1020A=