Canonical Allele Identifier: CA384386890

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703417T>A (hg19) ; chr12:g.39309615T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309615T>A , CM000674.2:g.39309615T>A	GRCh38
NC_000012.11:g.39703417T>A , CM000674.1:g.39703417T>A	GRCh37
NC_000012.10:g.37989684T>A	NCBI36
NG_017067.1:g.138776A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4248A>T MANE Select	ENSP00000354878.5:p.Arg1416Ser
ENST00000636569.1:c.4185A>T	ENSP00000490369.1:p.Arg1395Ser
ENST00000361418.9:c.4248A>T	ENSP00000354878.5:p.Arg1416Ser
ENST00000361961.7:c.4209A>T	ENSP00000354851.3:p.Arg1403Ser
ENST00000541463.6:c.4089A>T	ENSP00000438075.2:p.Arg1363Ser
ENST00000544797.6:c.4137A>T	ENSP00000445606.2:p.Arg1379Ser
ENST00000547733.1:n.1562A>T
ENST00000551264.5:c.1191A>T	ENSP00000448792.1:p.Arg397Ser
ENST00000552961.5:c.2150A>T
NM_001173463.1:c.4137A>T	NP_001166934.1:p.Arg1379Ser
NM_001173464.1:c.4248A>T	NP_001166935.1:p.Arg1416Ser
NM_001173465.1:c.4089A>T	NP_001166936.1:p.Arg1363Ser
NM_017641.3:c.4209A>T	NP_060111.2:p.Arg1403Ser
XM_005269007.1:c.4251A>T	XP_005269064.1:p.Arg1417Ser
XM_005269008.1:c.4236A>T	XP_005269065.1:p.Arg1412Ser
XM_005269009.1:c.4230A>T	XP_005269066.1:p.Arg1410Ser
XM_005269010.1:c.4212A>T	XP_005269067.1:p.Arg1404Ser
XM_005269011.1:c.4197A>T	XP_005269068.1:p.Arg1399Ser
XM_005269012.1:c.4122A>T	XP_005269069.1:p.Arg1374Ser
XM_005269013.1:c.4107A>T	XP_005269070.1:p.Arg1369Ser
XM_005269014.1:c.4068A>T	XP_005269071.1:p.Arg1356Ser
XM_006719493.1:c.4191A>T	XP_006719556.1:p.Arg1397Ser
XM_006719494.1:c.4119A>T	XP_006719557.1:p.Arg1373Ser
XM_006719496.1:c.4176A>T	XP_006719559.1:p.Arg1392Ser
XM_011538556.1:c.4182A>T	XP_011536858.1:p.Arg1394Ser
XM_005269007.3:c.4251A>T	XP_005269064.1:p.Arg1417Ser
XM_005269008.3:c.4236A>T	XP_005269065.1:p.Arg1412Ser
XM_005269009.3:c.4230A>T	XP_005269066.1:p.Arg1410Ser
XM_005269010.3:c.4212A>T	XP_005269067.1:p.Arg1404Ser
XM_005269011.3:c.4197A>T	XP_005269068.1:p.Arg1399Ser
XM_005269012.3:c.4122A>T	XP_005269069.1:p.Arg1374Ser
XM_005269013.3:c.4107A>T	XP_005269070.1:p.Arg1369Ser
XM_005269014.3:c.4068A>T	XP_005269071.1:p.Arg1356Ser
XM_006719493.3:c.4191A>T	XP_006719556.1:p.Arg1397Ser
XM_006719494.3:c.4119A>T	XP_006719557.1:p.Arg1373Ser
XM_011538556.3:c.4182A>T	XP_011536858.1:p.Arg1394Ser
XM_017019607.2:c.4197A>T	XP_016875096.1:p.Arg1399Ser
XM_017019608.2:c.4158A>T	XP_016875097.1:p.Arg1386Ser
XM_017019609.2:c.4047A>T	XP_016875098.1:p.Arg1349Ser
XM_017019610.2:c.4047A>T	XP_016875099.1:p.Arg1349Ser
XM_017019611.2:c.4029A>T	XP_016875100.1:p.Arg1343Ser
NM_001173463.2:c.4137A>T	NP_001166934.1:p.Arg1379Ser
NM_001173464.2:c.4248A>T MANE Select	NP_001166935.1:p.Arg1416Ser
NM_001173465.2:c.4089A>T	NP_001166936.1:p.Arg1363Ser
NM_017641.4:c.4209A>T	NP_060111.2:p.Arg1403Ser
NM_001378439.1:c.4251A>T	NP_001365368.1:p.Arg1417Ser
NM_001378440.1:c.4236A>T	NP_001365369.1:p.Arg1412Ser
NM_001378441.1:c.4212A>T	NP_001365370.1:p.Arg1404Ser