Canonical Allele Identifier: CA479233368
Gene: KIF21A HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.39703420G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.39309618G>A , CM000674.2:g.39309618G>A GRCh38
NC_000012.11:g.39703420G>A , CM000674.1:g.39703420G>A GRCh37
NC_000012.10:g.37989687G>A NCBI36
NG_017067.1:g.138773C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361418.10:c.4245C>T MANE Select ENSP00000354878.5:p.Ile1415=
ENST00000636569.1:c.4182C>T ENSP00000490369.1:p.Ile1394=
ENST00000361418.9:c.4245C>T ENSP00000354878.5:p.Ile1415=
ENST00000361961.7:c.4206C>T ENSP00000354851.3:p.Ile1402=
ENST00000541463.6:c.4086C>T ENSP00000438075.2:p.Ile1362=
ENST00000544797.6:c.4134C>T ENSP00000445606.2:p.Ile1378=
ENST00000547733.1:n.1559C>T
ENST00000551264.5:c.1188C>T ENSP00000448792.1:p.Ile396=
ENST00000552961.5:c.2147C>T
NM_001173463.1:c.4134C>T NP_001166934.1:p.Ile1378=
NM_001173464.1:c.4245C>T NP_001166935.1:p.Ile1415=
NM_001173465.1:c.4086C>T NP_001166936.1:p.Ile1362=
NM_017641.3:c.4206C>T NP_060111.2:p.Ile1402=
XM_005269007.1:c.4248C>T XP_005269064.1:p.Ile1416=
XM_005269008.1:c.4233C>T XP_005269065.1:p.Ile1411=
XM_005269009.1:c.4227C>T XP_005269066.1:p.Ile1409=
XM_005269010.1:c.4209C>T XP_005269067.1:p.Ile1403=
XM_005269011.1:c.4194C>T XP_005269068.1:p.Ile1398=
XM_005269012.1:c.4119C>T XP_005269069.1:p.Ile1373=
XM_005269013.1:c.4104C>T XP_005269070.1:p.Ile1368=
XM_005269014.1:c.4065C>T XP_005269071.1:p.Ile1355=
XM_006719493.1:c.4188C>T XP_006719556.1:p.Ile1396=
XM_006719494.1:c.4116C>T XP_006719557.1:p.Ile1372=
XM_006719496.1:c.4173C>T XP_006719559.1:p.Ile1391=
XM_011538556.1:c.4179C>T XP_011536858.1:p.Ile1393=
XM_005269007.3:c.4248C>T XP_005269064.1:p.Ile1416=
XM_005269008.3:c.4233C>T XP_005269065.1:p.Ile1411=
XM_005269009.3:c.4227C>T XP_005269066.1:p.Ile1409=
XM_005269010.3:c.4209C>T XP_005269067.1:p.Ile1403=
XM_005269011.3:c.4194C>T XP_005269068.1:p.Ile1398=
XM_005269012.3:c.4119C>T XP_005269069.1:p.Ile1373=
XM_005269013.3:c.4104C>T XP_005269070.1:p.Ile1368=
XM_005269014.3:c.4065C>T XP_005269071.1:p.Ile1355=
XM_006719493.3:c.4188C>T XP_006719556.1:p.Ile1396=
XM_006719494.3:c.4116C>T XP_006719557.1:p.Ile1372=
XM_011538556.3:c.4179C>T XP_011536858.1:p.Ile1393=
XM_017019607.2:c.4194C>T XP_016875096.1:p.Ile1398=
XM_017019608.2:c.4155C>T XP_016875097.1:p.Ile1385=
XM_017019609.2:c.4044C>T XP_016875098.1:p.Ile1348=
XM_017019610.2:c.4044C>T XP_016875099.1:p.Ile1348=
XM_017019611.2:c.4026C>T XP_016875100.1:p.Ile1342=
NM_001173463.2:c.4134C>T NP_001166934.1:p.Ile1378=
NM_001173464.2:c.4245C>T MANE Select NP_001166935.1:p.Ile1415=
NM_001173465.2:c.4086C>T NP_001166936.1:p.Ile1362=
NM_017641.4:c.4206C>T NP_060111.2:p.Ile1402=
NM_001378439.1:c.4248C>T NP_001365368.1:p.Ile1416=
NM_001378440.1:c.4233C>T NP_001365369.1:p.Ile1411=
NM_001378441.1:c.4209C>T NP_001365370.1:p.Ile1403=