Canonical Allele Identifier: CA1140228511

Gene: KIF26B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.245641362A= , CM000663.2:g.245641362A=	GRCh38
NC_000001.10:g.245804664A= , CM000663.1:g.245804664A=	GRCh37
NC_000001.9:g.243871287A=	NCBI36
NG_053061.1:g.491378A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407071.7:c.2099-4759A= MANE Select	ENSP00000385545.2:n.2099-4759A=
ENST00000366518.4:c.956-4759A=	ENSP00000355475.4:n.956-4759A=
ENST00000407071.6:c.2099-4759A=	ENSP00000385545.2:n.2099-4759A=
NM_018012.3:c.2099-4759A=	NP_060482.2:n.2099-4759A=
XM_011544214.1:c.1661-4759A=	XP_011542516.1:n.1661-4759A=
XM_011544215.1:c.1499-4759A=	XP_011542517.1:n.1499-4759A=
XM_011544216.1:c.1499-4759A=	XP_011542518.1:n.1499-4759A=
XM_011544217.1:c.1499-4759A=	XP_011542519.1:n.1499-4759A=
XM_011544218.1:c.956-4759A=	XP_011542520.1:n.956-4759A=
NM_018012.4:c.2099-4759A= MANE Select	NP_060482.2:n.2099-4759A=