Canonical Allele Identifier: CA344105327

Gene: KIF14

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200614398C>G , CM000663.2:g.200614398C>G	GRCh38
NC_000001.10:g.200583526C>G , CM000663.1:g.200583526C>G	GRCh37
NC_000001.9:g.198850149C>G	NCBI36
NG_042074.1:g.11337G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_014875.3:c.1375G>C MANE Select	NP_055690.1:p.Gly459Arg
ENST00000367350.5:c.1375G>C MANE Select	ENSP00000356319.4:p.Gly459Arg
NM_001305792.1:c.-19+957G>C	NP_001292721.1:n.-19+957G>C
NM_014875.2:c.1375G>C	NP_055690.1:p.Gly459Arg
ENST00000367350.4:c.1375G>C	ENSP00000356319.4:p.Gly459Arg
ENST00000614960.4:c.1375G>C	ENSP00000483069.1:p.Gly459Arg
XM_011510230.1:c.1375G>C	XP_011508532.1:p.Gly459Arg
XM_011510231.1:c.1375G>C	XP_011508533.1:p.Gly459Arg
XM_011510231.2:c.1375G>C	XP_011508533.1:p.Gly459Arg
XM_011510232.1:c.1375G>C	XP_011508534.1:p.Gly459Arg
XM_011510232.2:c.1375G>C	XP_011508534.1:p.Gly459Arg
XM_011510233.1:c.1291G>C	XP_011508535.1:p.Gly431Arg
XM_011510233.2:c.1291G>C	XP_011508535.1:p.Gly431Arg
XM_011510234.1:c.1276G>C	XP_011508536.1:p.Gly426Arg
XM_011510235.1:c.1003G>C	XP_011508537.1:p.Gly335Arg
XM_011510235.2:c.1003G>C	XP_011508537.1:p.Gly335Arg
XM_011510236.1:c.-19+957G>C	XP_011508538.1:n.-19+957G>C
XM_017003005.1:c.1375G>C	XP_016858494.1:p.Gly459Arg
XM_017003006.1:c.1246G>C	XP_016858495.1:p.Gly416Arg
XM_017003007.1:c.808G>C	XP_016858496.1:p.Gly270Arg