Canonical Allele Identifier: CA384386960

Gene: KIF21A

Linked Data

• COSMIC: COSM1676832 ; COSM1676833
• MyVariant Identifiers: chr12:g.39703426C>A (hg19) ; chr12:g.39309624C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309624C>A , CM000674.2:g.39309624C>A	GRCh38
NC_000012.11:g.39703426C>A , CM000674.1:g.39703426C>A	GRCh37
NC_000012.10:g.37989693C>A	NCBI36
NG_017067.1:g.138767G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4239G>T MANE Select	ENSP00000354878.5:p.Trp1413Cys
ENST00000636569.1:c.4176G>T	ENSP00000490369.1:p.Trp1392Cys
ENST00000361418.9:c.4239G>T	ENSP00000354878.5:p.Trp1413Cys
ENST00000361961.7:c.4200G>T	ENSP00000354851.3:p.Trp1400Cys
ENST00000541463.6:c.4080G>T	ENSP00000438075.2:p.Trp1360Cys
ENST00000544797.6:c.4128G>T	ENSP00000445606.2:p.Trp1376Cys
ENST00000547733.1:n.1553G>T
ENST00000551264.5:c.1182G>T	ENSP00000448792.1:p.Trp394Cys
ENST00000552961.5:c.2141G>T
NM_001173463.1:c.4128G>T	NP_001166934.1:p.Trp1376Cys
NM_001173464.1:c.4239G>T	NP_001166935.1:p.Trp1413Cys
NM_001173465.1:c.4080G>T	NP_001166936.1:p.Trp1360Cys
NM_017641.3:c.4200G>T	NP_060111.2:p.Trp1400Cys
XM_005269007.1:c.4242G>T	XP_005269064.1:p.Trp1414Cys
XM_005269008.1:c.4227G>T	XP_005269065.1:p.Trp1409Cys
XM_005269009.1:c.4221G>T	XP_005269066.1:p.Trp1407Cys
XM_005269010.1:c.4203G>T	XP_005269067.1:p.Trp1401Cys
XM_005269011.1:c.4188G>T	XP_005269068.1:p.Trp1396Cys
XM_005269012.1:c.4113G>T	XP_005269069.1:p.Trp1371Cys
XM_005269013.1:c.4098G>T	XP_005269070.1:p.Trp1366Cys
XM_005269014.1:c.4059G>T	XP_005269071.1:p.Trp1353Cys
XM_006719493.1:c.4182G>T	XP_006719556.1:p.Trp1394Cys
XM_006719494.1:c.4110G>T	XP_006719557.1:p.Trp1370Cys
XM_006719496.1:c.4167G>T	XP_006719559.1:p.Trp1389Cys
XM_011538556.1:c.4173G>T	XP_011536858.1:p.Trp1391Cys
XM_005269007.3:c.4242G>T	XP_005269064.1:p.Trp1414Cys
XM_005269008.3:c.4227G>T	XP_005269065.1:p.Trp1409Cys
XM_005269009.3:c.4221G>T	XP_005269066.1:p.Trp1407Cys
XM_005269010.3:c.4203G>T	XP_005269067.1:p.Trp1401Cys
XM_005269011.3:c.4188G>T	XP_005269068.1:p.Trp1396Cys
XM_005269012.3:c.4113G>T	XP_005269069.1:p.Trp1371Cys
XM_005269013.3:c.4098G>T	XP_005269070.1:p.Trp1366Cys
XM_005269014.3:c.4059G>T	XP_005269071.1:p.Trp1353Cys
XM_006719493.3:c.4182G>T	XP_006719556.1:p.Trp1394Cys
XM_006719494.3:c.4110G>T	XP_006719557.1:p.Trp1370Cys
XM_011538556.3:c.4173G>T	XP_011536858.1:p.Trp1391Cys
XM_017019607.2:c.4188G>T	XP_016875096.1:p.Trp1396Cys
XM_017019608.2:c.4149G>T	XP_016875097.1:p.Trp1383Cys
XM_017019609.2:c.4038G>T	XP_016875098.1:p.Trp1346Cys
XM_017019610.2:c.4038G>T	XP_016875099.1:p.Trp1346Cys
XM_017019611.2:c.4020G>T	XP_016875100.1:p.Trp1340Cys
NM_001173463.2:c.4128G>T	NP_001166934.1:p.Trp1376Cys
NM_001173464.2:c.4239G>T MANE Select	NP_001166935.1:p.Trp1413Cys
NM_001173465.2:c.4080G>T	NP_001166936.1:p.Trp1360Cys
NM_017641.4:c.4200G>T	NP_060111.2:p.Trp1400Cys
NM_001378439.1:c.4242G>T	NP_001365368.1:p.Trp1414Cys
NM_001378440.1:c.4227G>T	NP_001365369.1:p.Trp1409Cys
NM_001378441.1:c.4203G>T	NP_001365370.1:p.Trp1401Cys