Canonical Allele Identifier: CA1140228535

Gene: KIF26B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.245570306G= , CM000663.2:g.245570306G=	GRCh38
NC_000001.10:g.245733608G= , CM000663.1:g.245733608G=	GRCh37
NC_000001.9:g.243800231G=	NCBI36
NG_053061.1:g.420322G=

Transcript Alleles

HGVS	Amino-acid Change
NM_018012.4:c.1350+29356G= MANE Select	NP_060482.2:n.1350+29356G=
ENST00000407071.7:c.1350+29356G= MANE Select	ENSP00000385545.2:n.1350+29356G=
NM_018012.3:c.1350+29356G=	NP_060482.2:n.1350+29356G=
ENST00000366518.4:c.207+29356G=	ENSP00000355475.4:n.207+29356G=
ENST00000407071.6:c.1350+29356G=	ENSP00000385545.2:n.1350+29356G=
XM_011544214.1:c.912+29356G=	XP_011542516.1:n.912+29356G=
XM_011544215.1:c.750+29356G=	XP_011542517.1:n.750+29356G=
XM_011544216.1:c.750+29356G=	XP_011542518.1:n.750+29356G=
XM_011544217.1:c.750+29356G=	XP_011542519.1:n.750+29356G=
XM_011544218.1:c.207+29356G=	XP_011542520.1:n.207+29356G=