Canonical Allele Identifier: CA384387164

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703458A>T (hg19) ; chr12:g.39309656A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309656A>T , CM000674.2:g.39309656A>T	GRCh38
NC_000012.11:g.39703458A>T , CM000674.1:g.39703458A>T	GRCh37
NC_000012.10:g.37989725A>T	NCBI36
NG_017067.1:g.138735T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4207T>A MANE Select	ENSP00000354878.5:p.Phe1403Ile
ENST00000636569.1:c.4144T>A	ENSP00000490369.1:p.Phe1382Ile
ENST00000361418.9:c.4207T>A	ENSP00000354878.5:p.Phe1403Ile
ENST00000361961.7:c.4168T>A	ENSP00000354851.3:p.Phe1390Ile
ENST00000541463.6:c.4048T>A	ENSP00000438075.2:p.Phe1350Ile
ENST00000544797.6:c.4096T>A	ENSP00000445606.2:p.Phe1366Ile
ENST00000547733.1:n.1521T>A
ENST00000551264.5:c.1150T>A	ENSP00000448792.1:p.Phe384Ile
ENST00000552961.5:c.2109T>A
NM_001173463.1:c.4096T>A	NP_001166934.1:p.Phe1366Ile
NM_001173464.1:c.4207T>A	NP_001166935.1:p.Phe1403Ile
NM_001173465.1:c.4048T>A	NP_001166936.1:p.Phe1350Ile
NM_017641.3:c.4168T>A	NP_060111.2:p.Phe1390Ile
XM_005269007.1:c.4210T>A	XP_005269064.1:p.Phe1404Ile
XM_005269008.1:c.4195T>A	XP_005269065.1:p.Phe1399Ile
XM_005269009.1:c.4189T>A	XP_005269066.1:p.Phe1397Ile
XM_005269010.1:c.4171T>A	XP_005269067.1:p.Phe1391Ile
XM_005269011.1:c.4156T>A	XP_005269068.1:p.Phe1386Ile
XM_005269012.1:c.4081T>A	XP_005269069.1:p.Phe1361Ile
XM_005269013.1:c.4066T>A	XP_005269070.1:p.Phe1356Ile
XM_005269014.1:c.4027T>A	XP_005269071.1:p.Phe1343Ile
XM_006719493.1:c.4150T>A	XP_006719556.1:p.Phe1384Ile
XM_006719494.1:c.4078T>A	XP_006719557.1:p.Phe1360Ile
XM_006719496.1:c.4135T>A	XP_006719559.1:p.Phe1379Ile
XM_011538556.1:c.4141T>A	XP_011536858.1:p.Phe1381Ile
XM_005269007.3:c.4210T>A	XP_005269064.1:p.Phe1404Ile
XM_005269008.3:c.4195T>A	XP_005269065.1:p.Phe1399Ile
XM_005269009.3:c.4189T>A	XP_005269066.1:p.Phe1397Ile
XM_005269010.3:c.4171T>A	XP_005269067.1:p.Phe1391Ile
XM_005269011.3:c.4156T>A	XP_005269068.1:p.Phe1386Ile
XM_005269012.3:c.4081T>A	XP_005269069.1:p.Phe1361Ile
XM_005269013.3:c.4066T>A	XP_005269070.1:p.Phe1356Ile
XM_005269014.3:c.4027T>A	XP_005269071.1:p.Phe1343Ile
XM_006719493.3:c.4150T>A	XP_006719556.1:p.Phe1384Ile
XM_006719494.3:c.4078T>A	XP_006719557.1:p.Phe1360Ile
XM_011538556.3:c.4141T>A	XP_011536858.1:p.Phe1381Ile
XM_017019607.2:c.4156T>A	XP_016875096.1:p.Phe1386Ile
XM_017019608.2:c.4117T>A	XP_016875097.1:p.Phe1373Ile
XM_017019609.2:c.4006T>A	XP_016875098.1:p.Phe1336Ile
XM_017019610.2:c.4006T>A	XP_016875099.1:p.Phe1336Ile
XM_017019611.2:c.3988T>A	XP_016875100.1:p.Phe1330Ile
NM_001173463.2:c.4096T>A	NP_001166934.1:p.Phe1366Ile
NM_001173464.2:c.4207T>A MANE Select	NP_001166935.1:p.Phe1403Ile
NM_001173465.2:c.4048T>A	NP_001166936.1:p.Phe1350Ile
NM_017641.4:c.4168T>A	NP_060111.2:p.Phe1390Ile
NM_001378439.1:c.4210T>A	NP_001365368.1:p.Phe1404Ile
NM_001378440.1:c.4195T>A	NP_001365369.1:p.Phe1399Ile
NM_001378441.1:c.4171T>A	NP_001365370.1:p.Phe1391Ile