Canonical Allele Identifier: CA1317197

Gene: KIF14

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200569910C>A , CM000663.2:g.200569910C>A	GRCh38
NC_000001.10:g.200539038C>A , CM000663.1:g.200539038C>A	GRCh37
NC_000001.9:g.198805661C>A	NCBI36
NG_042074.1:g.55825G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014875.3:c.3661+1G>T MANE Select	NP_055690.1:n.3661+1G>T
ENST00000367350.5:c.3661+1G>T MANE Select	ENSP00000356319.4:n.3661+1G>T
NM_001305792.1:c.2188+1G>T	NP_001292721.1:n.2188+1G>T
NM_014875.2:c.3661+1G>T	NP_055690.1:n.3661+1G>T
ENST00000367350.4:c.3661+1G>T	ENSP00000356319.4:n.3661+1G>T
ENST00000614960.4:c.3661+1G>T	ENSP00000483069.1:n.3661+1G>T
XM_011510230.1:c.3661+1G>T	XP_011508532.1:n.3661+1G>T
XM_011510231.1:c.3661+1G>T	XP_011508533.1:n.3661+1G>T
XM_011510231.2:c.3661+1G>T	XP_011508533.1:n.3661+1G>T
XM_011510232.1:c.3661+1G>T	XP_011508534.1:n.3661+1G>T
XM_011510232.2:c.3661+1G>T	XP_011508534.1:n.3661+1G>T
XM_011510233.1:c.3577+1G>T	XP_011508535.1:n.3577+1G>T
XM_011510233.2:c.3577+1G>T	XP_011508535.1:n.3577+1G>T
XM_011510234.1:c.3562+1G>T	XP_011508536.1:n.3562+1G>T
XM_011510235.1:c.3289+1G>T	XP_011508537.1:n.3289+1G>T
XM_011510235.2:c.3289+1G>T	XP_011508537.1:n.3289+1G>T
XM_011510236.1:c.2188+1G>T	XP_011508538.1:n.2188+1G>T
XM_017003005.1:c.3661+1G>T	XP_016858494.1:n.3661+1G>T
XM_017003006.1:c.3532+1G>T	XP_016858495.1:n.3532+1G>T
XM_017003007.1:c.3094+1G>T	XP_016858496.1:n.3094+1G>T