Canonical Allele Identifier: CA1231332829
Gene: KIF26B HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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