Canonical Allele Identifier: CA1219391229

Gene: KIF14

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200603833A= , CM000663.2:g.200603833A=	GRCh38
NC_000001.10:g.200572961A= , CM000663.1:g.200572961A=	GRCh37
NC_000001.9:g.198839584A=	NCBI36
NG_042074.1:g.21902T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367350.5:c.1863+6T= MANE Select	ENSP00000356319.4:n.1863+6T=
ENST00000367350.4:c.1863+6T=	ENSP00000356319.4:n.1863+6T=
ENST00000614960.4:c.1863+6T=	ENSP00000483069.1:n.1863+6T=
NM_001305792.1:c.390+6T=	NP_001292721.1:n.390+6T=
NM_014875.2:c.1863+6T=	NP_055690.1:n.1863+6T=
XM_011510230.1:c.1863+6T=	XP_011508532.1:n.1863+6T=
XM_011510231.1:c.1863+6T=	XP_011508533.1:n.1863+6T=
XM_011510232.1:c.1863+6T=	XP_011508534.1:n.1863+6T=
XM_011510233.1:c.1779+6T=	XP_011508535.1:n.1779+6T=
XM_011510234.1:c.1764+6T=	XP_011508536.1:n.1764+6T=
XM_011510235.1:c.1491+6T=	XP_011508537.1:n.1491+6T=
XM_011510236.1:c.390+6T=	XP_011508538.1:n.390+6T=
XM_011510231.2:c.1863+6T=	XP_011508533.1:n.1863+6T=
XM_011510232.2:c.1863+6T=	XP_011508534.1:n.1863+6T=
XM_011510233.2:c.1779+6T=	XP_011508535.1:n.1779+6T=
XM_011510235.2:c.1491+6T=	XP_011508537.1:n.1491+6T=
XM_017003005.1:c.1863+6T=	XP_016858494.1:n.1863+6T=
XM_017003006.1:c.1734+6T=	XP_016858495.1:n.1734+6T=
XM_017003007.1:c.1296+6T=	XP_016858496.1:n.1296+6T=
NM_014875.3:c.1863+6T= MANE Select	NP_055690.1:n.1863+6T=