Canonical Allele Identifier: CA2030565397
Gene: KIF21A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.39309590G= , CM000674.2:g.39309590G= GRCh38
NC_000012.11:g.39703392G= , CM000674.1:g.39703392G= GRCh37
NC_000012.10:g.37989659G= NCBI36
NG_017067.1:g.138801C=

Transcript Alleles

HGVS Amino-acid change
ENST00000361418.10:c.4273C= MANE Select ENSP00000354878.5:p.Leu1425=
ENST00000636569.1:c.4210C= ENSP00000490369.1:p.Leu1404=
ENST00000361418.9:c.4273C= ENSP00000354878.5:p.Leu1425=
ENST00000361961.7:c.4234C= ENSP00000354851.3:p.Leu1412=
ENST00000541463.6:c.4114C= ENSP00000438075.2:p.Leu1372=
ENST00000544797.6:c.4162C= ENSP00000445606.2:p.Leu1388=
ENST00000547733.1:n.1587C=
ENST00000551264.5:c.1216C= ENSP00000448792.1:p.Leu406=
ENST00000552961.5:c.2175C=
NM_001173463.1:c.4162C= NP_001166934.1:p.Leu1388=
NM_001173464.1:c.4273C= NP_001166935.1:p.Leu1425=
NM_001173465.1:c.4114C= NP_001166936.1:p.Leu1372=
NM_017641.3:c.4234C= NP_060111.2:p.Leu1412=
XM_005269007.1:c.4276C= XP_005269064.1:p.Leu1426=
XM_005269008.1:c.4261C= XP_005269065.1:p.Leu1421=
XM_005269009.1:c.4255C= XP_005269066.1:p.Leu1419=
XM_005269010.1:c.4237C= XP_005269067.1:p.Leu1413=
XM_005269011.1:c.4222C= XP_005269068.1:p.Leu1408=
XM_005269012.1:c.4147C= XP_005269069.1:p.Leu1383=
XM_005269013.1:c.4132C= XP_005269070.1:p.Leu1378=
XM_005269014.1:c.4093C= XP_005269071.1:p.Leu1365=
XM_006719493.1:c.4216C= XP_006719556.1:p.Leu1406=
XM_006719494.1:c.4144C= XP_006719557.1:p.Leu1382=
XM_006719496.1:c.4201C= XP_006719559.1:p.Leu1401=
XM_011538556.1:c.4207C= XP_011536858.1:p.Leu1403=
XM_005269007.3:c.4276C= XP_005269064.1:p.Leu1426=
XM_005269008.3:c.4261C= XP_005269065.1:p.Leu1421=
XM_005269009.3:c.4255C= XP_005269066.1:p.Leu1419=
XM_005269010.3:c.4237C= XP_005269067.1:p.Leu1413=
XM_005269011.3:c.4222C= XP_005269068.1:p.Leu1408=
XM_005269012.3:c.4147C= XP_005269069.1:p.Leu1383=
XM_005269013.3:c.4132C= XP_005269070.1:p.Leu1378=
XM_005269014.3:c.4093C= XP_005269071.1:p.Leu1365=
XM_006719493.3:c.4216C= XP_006719556.1:p.Leu1406=
XM_006719494.3:c.4144C= XP_006719557.1:p.Leu1382=
XM_011538556.3:c.4207C= XP_011536858.1:p.Leu1403=
XM_017019607.2:c.4222C= XP_016875096.1:p.Leu1408=
XM_017019608.2:c.4183C= XP_016875097.1:p.Leu1395=
XM_017019609.2:c.4072C= XP_016875098.1:p.Leu1358=
XM_017019610.2:c.4072C= XP_016875099.1:p.Leu1358=
XM_017019611.2:c.4054C= XP_016875100.1:p.Leu1352=
NM_001173463.2:c.4162C= NP_001166934.1:p.Leu1388=
NM_001173464.2:c.4273C= MANE Select NP_001166935.1:p.Leu1425=
NM_001173465.2:c.4114C= NP_001166936.1:p.Leu1372=
NM_017641.4:c.4234C= NP_060111.2:p.Leu1412=
NM_001378439.1:c.4276C= NP_001365368.1:p.Leu1426=
NM_001378440.1:c.4261C= NP_001365369.1:p.Leu1421=
NM_001378441.1:c.4237C= NP_001365370.1:p.Leu1413=