Canonical Allele Identifier: CA344107733

Gene: KIF14

Linked Data

• MyVariant Identifiers: chr1:g.200522681C>A (hg19) ; chr1:g.200553553C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.200553553C>A , CM000663.2:g.200553553C>A	GRCh38
NC_000001.10:g.200522681C>A , CM000663.1:g.200522681C>A	GRCh37
NC_000001.9:g.198789304C>A	NCBI36
NG_042074.1:g.72182G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367350.5:c.4782G>T MANE Select	ENSP00000356319.4:p.Trp1594Cys
ENST00000367350.4:c.4782G>T	ENSP00000356319.4:p.Trp1594Cys
ENST00000614960.4:c.4782G>T	ENSP00000483069.1:p.Trp1594Cys
NM_001305792.1:c.3309G>T	NP_001292721.1:p.Trp1103Cys
NM_014875.2:c.4782G>T	NP_055690.1:p.Trp1594Cys
XM_011510230.1:c.4782G>T	XP_011508532.1:p.Trp1594Cys
XM_011510231.1:c.4782G>T	XP_011508533.1:p.Trp1594Cys
XM_011510232.1:c.4782G>T	XP_011508534.1:p.Trp1594Cys
XM_011510233.1:c.4698G>T	XP_011508535.1:p.Trp1566Cys
XM_011510234.1:c.4683G>T	XP_011508536.1:p.Trp1561Cys
XM_011510235.1:c.4410G>T	XP_011508537.1:p.Trp1470Cys
XM_011510236.1:c.3309G>T	XP_011508538.1:p.Trp1103Cys
XM_011510231.2:c.4782G>T	XP_011508533.1:p.Trp1594Cys
XM_011510232.2:c.4782G>T	XP_011508534.1:p.Trp1594Cys
XM_011510233.2:c.4698G>T	XP_011508535.1:p.Trp1566Cys
XM_011510235.2:c.4410G>T	XP_011508537.1:p.Trp1470Cys
XM_017003005.1:c.4782G>T	XP_016858494.1:p.Trp1594Cys
XM_017003006.1:c.4653G>T	XP_016858495.1:p.Trp1551Cys
XM_017003007.1:c.4215G>T	XP_016858496.1:p.Trp1405Cys
NM_014875.3:c.4782G>T MANE Select	NP_055690.1:p.Trp1594Cys