Canonical Allele Identifier: CA384387185

Gene: KIF21A

Linked Data

• COSMIC: COSM5480343 ; COSM5480344
• MyVariant Identifiers: chr12:g.39703462C>A (hg19) ; chr12:g.39309660C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309660C>A , CM000674.2:g.39309660C>A	GRCh38
NC_000012.11:g.39703462C>A , CM000674.1:g.39703462C>A	GRCh37
NC_000012.10:g.37989729C>A	NCBI36
NG_017067.1:g.138731G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4203G>T MANE Select	ENSP00000354878.5:p.Leu1401Phe
ENST00000636569.1:c.4140G>T	ENSP00000490369.1:p.Leu1380Phe
ENST00000361418.9:c.4203G>T	ENSP00000354878.5:p.Leu1401Phe
ENST00000361961.7:c.4164G>T	ENSP00000354851.3:p.Leu1388Phe
ENST00000541463.6:c.4044G>T	ENSP00000438075.2:p.Leu1348Phe
ENST00000544797.6:c.4092G>T	ENSP00000445606.2:p.Leu1364Phe
ENST00000547733.1:n.1517G>T
ENST00000551264.5:c.1146G>T	ENSP00000448792.1:p.Leu382Phe
ENST00000552961.5:c.2105G>T
NM_001173463.1:c.4092G>T	NP_001166934.1:p.Leu1364Phe
NM_001173464.1:c.4203G>T	NP_001166935.1:p.Leu1401Phe
NM_001173465.1:c.4044G>T	NP_001166936.1:p.Leu1348Phe
NM_017641.3:c.4164G>T	NP_060111.2:p.Leu1388Phe
XM_005269007.1:c.4206G>T	XP_005269064.1:p.Leu1402Phe
XM_005269008.1:c.4191G>T	XP_005269065.1:p.Leu1397Phe
XM_005269009.1:c.4185G>T	XP_005269066.1:p.Leu1395Phe
XM_005269010.1:c.4167G>T	XP_005269067.1:p.Leu1389Phe
XM_005269011.1:c.4152G>T	XP_005269068.1:p.Leu1384Phe
XM_005269012.1:c.4077G>T	XP_005269069.1:p.Leu1359Phe
XM_005269013.1:c.4062G>T	XP_005269070.1:p.Leu1354Phe
XM_005269014.1:c.4023G>T	XP_005269071.1:p.Leu1341Phe
XM_006719493.1:c.4146G>T	XP_006719556.1:p.Leu1382Phe
XM_006719494.1:c.4074G>T	XP_006719557.1:p.Leu1358Phe
XM_006719496.1:c.4131G>T	XP_006719559.1:p.Leu1377Phe
XM_011538556.1:c.4137G>T	XP_011536858.1:p.Leu1379Phe
XM_005269007.3:c.4206G>T	XP_005269064.1:p.Leu1402Phe
XM_005269008.3:c.4191G>T	XP_005269065.1:p.Leu1397Phe
XM_005269009.3:c.4185G>T	XP_005269066.1:p.Leu1395Phe
XM_005269010.3:c.4167G>T	XP_005269067.1:p.Leu1389Phe
XM_005269011.3:c.4152G>T	XP_005269068.1:p.Leu1384Phe
XM_005269012.3:c.4077G>T	XP_005269069.1:p.Leu1359Phe
XM_005269013.3:c.4062G>T	XP_005269070.1:p.Leu1354Phe
XM_005269014.3:c.4023G>T	XP_005269071.1:p.Leu1341Phe
XM_006719493.3:c.4146G>T	XP_006719556.1:p.Leu1382Phe
XM_006719494.3:c.4074G>T	XP_006719557.1:p.Leu1358Phe
XM_011538556.3:c.4137G>T	XP_011536858.1:p.Leu1379Phe
XM_017019607.2:c.4152G>T	XP_016875096.1:p.Leu1384Phe
XM_017019608.2:c.4113G>T	XP_016875097.1:p.Leu1371Phe
XM_017019609.2:c.4002G>T	XP_016875098.1:p.Leu1334Phe
XM_017019610.2:c.4002G>T	XP_016875099.1:p.Leu1334Phe
XM_017019611.2:c.3984G>T	XP_016875100.1:p.Leu1328Phe
NM_001173463.2:c.4092G>T	NP_001166934.1:p.Leu1364Phe
NM_001173464.2:c.4203G>T MANE Select	NP_001166935.1:p.Leu1401Phe
NM_001173465.2:c.4044G>T	NP_001166936.1:p.Leu1348Phe
NM_017641.4:c.4164G>T	NP_060111.2:p.Leu1388Phe
NM_001378439.1:c.4206G>T	NP_001365368.1:p.Leu1402Phe
NM_001378440.1:c.4191G>T	NP_001365369.1:p.Leu1397Phe
NM_001378441.1:c.4167G>T	NP_001365370.1:p.Leu1389Phe