Canonical Allele Identifier: CA35948416

Gene: KIF14

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200565669C>A , CM000663.2:g.200565669C>A	GRCh38
NC_000001.10:g.200534797C>A , CM000663.1:g.200534797C>A	GRCh37
NC_000001.9:g.198801420C>A	NCBI36
NG_042074.1:g.60066G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014875.3:c.3662G>T MANE Select	NP_055690.1:p.Gly1221Val
ENST00000367350.5:c.3662G>T MANE Select	ENSP00000356319.4:p.Gly1221Val
NM_001305792.1:c.2189G>T	NP_001292721.1:p.Gly730Val
NM_014875.2:c.3662G>T	NP_055690.1:p.Gly1221Val
ENST00000367350.4:c.3662G>T	ENSP00000356319.4:p.Gly1221Val
ENST00000614960.4:c.3662G>T	ENSP00000483069.1:p.Gly1221Val
XM_011510230.1:c.3662G>T	XP_011508532.1:p.Gly1221Val
XM_011510231.1:c.3662G>T	XP_011508533.1:p.Gly1221Val
XM_011510231.2:c.3662G>T	XP_011508533.1:p.Gly1221Val
XM_011510232.1:c.3662G>T	XP_011508534.1:p.Gly1221Val
XM_011510232.2:c.3662G>T	XP_011508534.1:p.Gly1221Val
XM_011510233.1:c.3578G>T	XP_011508535.1:p.Gly1193Val
XM_011510233.2:c.3578G>T	XP_011508535.1:p.Gly1193Val
XM_011510234.1:c.3563G>T	XP_011508536.1:p.Gly1188Val
XM_011510235.1:c.3290G>T	XP_011508537.1:p.Gly1097Val
XM_011510235.2:c.3290G>T	XP_011508537.1:p.Gly1097Val
XM_011510236.1:c.2189G>T	XP_011508538.1:p.Gly730Val
XM_017003005.1:c.3662G>T	XP_016858494.1:p.Gly1221Val
XM_017003006.1:c.3533G>T	XP_016858495.1:p.Gly1178Val
XM_017003007.1:c.3095G>T	XP_016858496.1:p.Gly1032Val