Canonical Allele Identifier: CA384387061

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703442G>C (hg19) ; chr12:g.39309640G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309640G>C , CM000674.2:g.39309640G>C	GRCh38
NC_000012.11:g.39703442G>C , CM000674.1:g.39703442G>C	GRCh37
NC_000012.10:g.37989709G>C	NCBI36
NG_017067.1:g.138751C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4223C>G MANE Select	ENSP00000354878.5:p.Ser1408Cys
ENST00000636569.1:c.4160C>G	ENSP00000490369.1:p.Ser1387Cys
ENST00000361418.9:c.4223C>G	ENSP00000354878.5:p.Ser1408Cys
ENST00000361961.7:c.4184C>G	ENSP00000354851.3:p.Ser1395Cys
ENST00000541463.6:c.4064C>G	ENSP00000438075.2:p.Ser1355Cys
ENST00000544797.6:c.4112C>G	ENSP00000445606.2:p.Ser1371Cys
ENST00000547733.1:n.1537C>G
ENST00000551264.5:c.1166C>G	ENSP00000448792.1:p.Ser389Cys
ENST00000552961.5:c.2125C>G
NM_001173463.1:c.4112C>G	NP_001166934.1:p.Ser1371Cys
NM_001173464.1:c.4223C>G	NP_001166935.1:p.Ser1408Cys
NM_001173465.1:c.4064C>G	NP_001166936.1:p.Ser1355Cys
NM_017641.3:c.4184C>G	NP_060111.2:p.Ser1395Cys
XM_005269007.1:c.4226C>G	XP_005269064.1:p.Ser1409Cys
XM_005269008.1:c.4211C>G	XP_005269065.1:p.Ser1404Cys
XM_005269009.1:c.4205C>G	XP_005269066.1:p.Ser1402Cys
XM_005269010.1:c.4187C>G	XP_005269067.1:p.Ser1396Cys
XM_005269011.1:c.4172C>G	XP_005269068.1:p.Ser1391Cys
XM_005269012.1:c.4097C>G	XP_005269069.1:p.Ser1366Cys
XM_005269013.1:c.4082C>G	XP_005269070.1:p.Ser1361Cys
XM_005269014.1:c.4043C>G	XP_005269071.1:p.Ser1348Cys
XM_006719493.1:c.4166C>G	XP_006719556.1:p.Ser1389Cys
XM_006719494.1:c.4094C>G	XP_006719557.1:p.Ser1365Cys
XM_006719496.1:c.4151C>G	XP_006719559.1:p.Ser1384Cys
XM_011538556.1:c.4157C>G	XP_011536858.1:p.Ser1386Cys
XM_005269007.3:c.4226C>G	XP_005269064.1:p.Ser1409Cys
XM_005269008.3:c.4211C>G	XP_005269065.1:p.Ser1404Cys
XM_005269009.3:c.4205C>G	XP_005269066.1:p.Ser1402Cys
XM_005269010.3:c.4187C>G	XP_005269067.1:p.Ser1396Cys
XM_005269011.3:c.4172C>G	XP_005269068.1:p.Ser1391Cys
XM_005269012.3:c.4097C>G	XP_005269069.1:p.Ser1366Cys
XM_005269013.3:c.4082C>G	XP_005269070.1:p.Ser1361Cys
XM_005269014.3:c.4043C>G	XP_005269071.1:p.Ser1348Cys
XM_006719493.3:c.4166C>G	XP_006719556.1:p.Ser1389Cys
XM_006719494.3:c.4094C>G	XP_006719557.1:p.Ser1365Cys
XM_011538556.3:c.4157C>G	XP_011536858.1:p.Ser1386Cys
XM_017019607.2:c.4172C>G	XP_016875096.1:p.Ser1391Cys
XM_017019608.2:c.4133C>G	XP_016875097.1:p.Ser1378Cys
XM_017019609.2:c.4022C>G	XP_016875098.1:p.Ser1341Cys
XM_017019610.2:c.4022C>G	XP_016875099.1:p.Ser1341Cys
XM_017019611.2:c.4004C>G	XP_016875100.1:p.Ser1335Cys
NM_001173463.2:c.4112C>G	NP_001166934.1:p.Ser1371Cys
NM_001173464.2:c.4223C>G MANE Select	NP_001166935.1:p.Ser1408Cys
NM_001173465.2:c.4064C>G	NP_001166936.1:p.Ser1355Cys
NM_017641.4:c.4184C>G	NP_060111.2:p.Ser1395Cys
NM_001378439.1:c.4226C>G	NP_001365368.1:p.Ser1409Cys
NM_001378440.1:c.4211C>G	NP_001365369.1:p.Ser1404Cys
NM_001378441.1:c.4187C>G	NP_001365370.1:p.Ser1396Cys