Canonical Allele Identifier: CA384387099

Gene: KIF21A

Linked Data

• dbSNP Id: rs2137324413
• MyVariant Identifiers: chr12:g.39703448G>A (hg19) ; chr12:g.39309646G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309646G>A , CM000674.2:g.39309646G>A	GRCh38
NC_000012.11:g.39703448G>A , CM000674.1:g.39703448G>A	GRCh37
NC_000012.10:g.37989715G>A	NCBI36
NG_017067.1:g.138745C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4217C>T MANE Select	ENSP00000354878.5:p.Ser1406Leu
ENST00000636569.1:c.4154C>T	ENSP00000490369.1:p.Ser1385Leu
ENST00000361418.9:c.4217C>T	ENSP00000354878.5:p.Ser1406Leu
ENST00000361961.7:c.4178C>T	ENSP00000354851.3:p.Ser1393Leu
ENST00000541463.6:c.4058C>T	ENSP00000438075.2:p.Ser1353Leu
ENST00000544797.6:c.4106C>T	ENSP00000445606.2:p.Ser1369Leu
ENST00000547733.1:n.1531C>T
ENST00000551264.5:c.1160C>T	ENSP00000448792.1:p.Ser387Leu
ENST00000552961.5:c.2119C>T
NM_001173463.1:c.4106C>T	NP_001166934.1:p.Ser1369Leu
NM_001173464.1:c.4217C>T	NP_001166935.1:p.Ser1406Leu
NM_001173465.1:c.4058C>T	NP_001166936.1:p.Ser1353Leu
NM_017641.3:c.4178C>T	NP_060111.2:p.Ser1393Leu
XM_005269007.1:c.4220C>T	XP_005269064.1:p.Ser1407Leu
XM_005269008.1:c.4205C>T	XP_005269065.1:p.Ser1402Leu
XM_005269009.1:c.4199C>T	XP_005269066.1:p.Ser1400Leu
XM_005269010.1:c.4181C>T	XP_005269067.1:p.Ser1394Leu
XM_005269011.1:c.4166C>T	XP_005269068.1:p.Ser1389Leu
XM_005269012.1:c.4091C>T	XP_005269069.1:p.Ser1364Leu
XM_005269013.1:c.4076C>T	XP_005269070.1:p.Ser1359Leu
XM_005269014.1:c.4037C>T	XP_005269071.1:p.Ser1346Leu
XM_006719493.1:c.4160C>T	XP_006719556.1:p.Ser1387Leu
XM_006719494.1:c.4088C>T	XP_006719557.1:p.Ser1363Leu
XM_006719496.1:c.4145C>T	XP_006719559.1:p.Ser1382Leu
XM_011538556.1:c.4151C>T	XP_011536858.1:p.Ser1384Leu
XM_005269007.3:c.4220C>T	XP_005269064.1:p.Ser1407Leu
XM_005269008.3:c.4205C>T	XP_005269065.1:p.Ser1402Leu
XM_005269009.3:c.4199C>T	XP_005269066.1:p.Ser1400Leu
XM_005269010.3:c.4181C>T	XP_005269067.1:p.Ser1394Leu
XM_005269011.3:c.4166C>T	XP_005269068.1:p.Ser1389Leu
XM_005269012.3:c.4091C>T	XP_005269069.1:p.Ser1364Leu
XM_005269013.3:c.4076C>T	XP_005269070.1:p.Ser1359Leu
XM_005269014.3:c.4037C>T	XP_005269071.1:p.Ser1346Leu
XM_006719493.3:c.4160C>T	XP_006719556.1:p.Ser1387Leu
XM_006719494.3:c.4088C>T	XP_006719557.1:p.Ser1363Leu
XM_011538556.3:c.4151C>T	XP_011536858.1:p.Ser1384Leu
XM_017019607.2:c.4166C>T	XP_016875096.1:p.Ser1389Leu
XM_017019608.2:c.4127C>T	XP_016875097.1:p.Ser1376Leu
XM_017019609.2:c.4016C>T	XP_016875098.1:p.Ser1339Leu
XM_017019610.2:c.4016C>T	XP_016875099.1:p.Ser1339Leu
XM_017019611.2:c.3998C>T	XP_016875100.1:p.Ser1333Leu
NM_001173463.2:c.4106C>T	NP_001166934.1:p.Ser1369Leu
NM_001173464.2:c.4217C>T MANE Select	NP_001166935.1:p.Ser1406Leu
NM_001173465.2:c.4058C>T	NP_001166936.1:p.Ser1353Leu
NM_017641.4:c.4178C>T	NP_060111.2:p.Ser1393Leu
NM_001378439.1:c.4220C>T	NP_001365368.1:p.Ser1407Leu
NM_001378440.1:c.4205C>T	NP_001365369.1:p.Ser1402Leu
NM_001378441.1:c.4181C>T	NP_001365370.1:p.Ser1394Leu