Canonical Allele Identifier: CA1139838696

Gene: KIF26B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.245686793C= , CM000663.2:g.245686793C=	GRCh38
NC_000001.10:g.245850095C= , CM000663.1:g.245850095C=	GRCh37
NC_000001.9:g.243916718C=	NCBI36
NG_053061.1:g.536809C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407071.7:c.3810C= MANE Select	ENSP00000385545.2:p.Asp1270=
ENST00000366518.4:c.2667C=	ENSP00000355475.4:p.Asp889=
ENST00000407071.6:c.3810C=	ENSP00000385545.2:p.Asp1270=
ENST00000483253.1:n.1741C=
NM_018012.3:c.3810C=	NP_060482.2:p.Asp1270=
XM_011544214.1:c.3372C=	XP_011542516.1:p.Asp1124=
XM_011544215.1:c.3210C=	XP_011542517.1:p.Asp1070=
XM_011544216.1:c.3210C=	XP_011542518.1:p.Asp1070=
XM_011544217.1:c.3210C=	XP_011542519.1:p.Asp1070=
XM_011544218.1:c.2667C=	XP_011542520.1:p.Asp889=
NM_018012.4:c.3810C= MANE Select	NP_060482.2:p.Asp1270=
XR_001737764.2:n.1715-3410G=