Canonical Allele Identifier: CA2030565562
Gene: KIF21A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.39309691A= , CM000674.2:g.39309691A= GRCh38
NC_000012.11:g.39703493A= , CM000674.1:g.39703493A= GRCh37
NC_000012.10:g.37989760A= NCBI36
NG_017067.1:g.138700T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361418.10:c.4172T= MANE Select ENSP00000354878.5:p.Val1391=
ENST00000636569.1:c.4109T= ENSP00000490369.1:p.Val1370=
ENST00000361418.9:c.4172T= ENSP00000354878.5:p.Val1391=
ENST00000361961.7:c.4133T= ENSP00000354851.3:p.Val1378=
ENST00000541463.6:c.4013T= ENSP00000438075.2:p.Val1338=
ENST00000544797.6:c.4061T= ENSP00000445606.2:p.Val1354=
ENST00000547733.1:n.1486T=
ENST00000551264.5:c.1115T= ENSP00000448792.1:p.Val372=
ENST00000552961.5:c.2074T=
NM_001173463.1:c.4061T= NP_001166934.1:p.Val1354=
NM_001173464.1:c.4172T= NP_001166935.1:p.Val1391=
NM_001173465.1:c.4013T= NP_001166936.1:p.Val1338=
NM_017641.3:c.4133T= NP_060111.2:p.Val1378=
XM_005269007.1:c.4175T= XP_005269064.1:p.Val1392=
XM_005269008.1:c.4160T= XP_005269065.1:p.Val1387=
XM_005269009.1:c.4154T= XP_005269066.1:p.Val1385=
XM_005269010.1:c.4136T= XP_005269067.1:p.Val1379=
XM_005269011.1:c.4121T= XP_005269068.1:p.Val1374=
XM_005269012.1:c.4046T= XP_005269069.1:p.Val1349=
XM_005269013.1:c.4031T= XP_005269070.1:p.Val1344=
XM_005269014.1:c.3992T= XP_005269071.1:p.Val1331=
XM_006719493.1:c.4115T= XP_006719556.1:p.Val1372=
XM_006719494.1:c.4043T= XP_006719557.1:p.Val1348=
XM_006719496.1:c.4100T= XP_006719559.1:p.Val1367=
XM_011538556.1:c.4106T= XP_011536858.1:p.Val1369=
XM_005269007.3:c.4175T= XP_005269064.1:p.Val1392=
XM_005269008.3:c.4160T= XP_005269065.1:p.Val1387=
XM_005269009.3:c.4154T= XP_005269066.1:p.Val1385=
XM_005269010.3:c.4136T= XP_005269067.1:p.Val1379=
XM_005269011.3:c.4121T= XP_005269068.1:p.Val1374=
XM_005269012.3:c.4046T= XP_005269069.1:p.Val1349=
XM_005269013.3:c.4031T= XP_005269070.1:p.Val1344=
XM_005269014.3:c.3992T= XP_005269071.1:p.Val1331=
XM_006719493.3:c.4115T= XP_006719556.1:p.Val1372=
XM_006719494.3:c.4043T= XP_006719557.1:p.Val1348=
XM_011538556.3:c.4106T= XP_011536858.1:p.Val1369=
XM_017019607.2:c.4121T= XP_016875096.1:p.Val1374=
XM_017019608.2:c.4082T= XP_016875097.1:p.Val1361=
XM_017019609.2:c.3971T= XP_016875098.1:p.Val1324=
XM_017019610.2:c.3971T= XP_016875099.1:p.Val1324=
XM_017019611.2:c.3953T= XP_016875100.1:p.Val1318=
NM_001173463.2:c.4061T= NP_001166934.1:p.Val1354=
NM_001173464.2:c.4172T= MANE Select NP_001166935.1:p.Val1391=
NM_001173465.2:c.4013T= NP_001166936.1:p.Val1338=
NM_017641.4:c.4133T= NP_060111.2:p.Val1378=
NM_001378439.1:c.4175T= NP_001365368.1:p.Val1392=
NM_001378440.1:c.4160T= NP_001365369.1:p.Val1387=
NM_001378441.1:c.4136T= NP_001365370.1:p.Val1379=