Canonical Allele Identifier: CA384387181
Gene: KIF21A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.39309659C>G , CM000674.2:g.39309659C>G GRCh38
NC_000012.11:g.39703461C>G , CM000674.1:g.39703461C>G GRCh37
NC_000012.10:g.37989728C>G NCBI36
NG_017067.1:g.138732G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361418.10:c.4204G>C MANE Select ENSP00000354878.5:p.Val1402Leu
ENST00000636569.1:c.4141G>C ENSP00000490369.1:p.Val1381Leu
ENST00000361418.9:c.4204G>C ENSP00000354878.5:p.Val1402Leu
ENST00000361961.7:c.4165G>C ENSP00000354851.3:p.Val1389Leu
ENST00000541463.6:c.4045G>C ENSP00000438075.2:p.Val1349Leu
ENST00000544797.6:c.4093G>C ENSP00000445606.2:p.Val1365Leu
ENST00000547733.1:n.1518G>C
ENST00000551264.5:c.1147G>C ENSP00000448792.1:p.Val383Leu
ENST00000552961.5:c.2106G>C
NM_001173463.1:c.4093G>C NP_001166934.1:p.Val1365Leu
NM_001173464.1:c.4204G>C NP_001166935.1:p.Val1402Leu
NM_001173465.1:c.4045G>C NP_001166936.1:p.Val1349Leu
NM_017641.3:c.4165G>C NP_060111.2:p.Val1389Leu
XM_005269007.1:c.4207G>C XP_005269064.1:p.Val1403Leu
XM_005269008.1:c.4192G>C XP_005269065.1:p.Val1398Leu
XM_005269009.1:c.4186G>C XP_005269066.1:p.Val1396Leu
XM_005269010.1:c.4168G>C XP_005269067.1:p.Val1390Leu
XM_005269011.1:c.4153G>C XP_005269068.1:p.Val1385Leu
XM_005269012.1:c.4078G>C XP_005269069.1:p.Val1360Leu
XM_005269013.1:c.4063G>C XP_005269070.1:p.Val1355Leu
XM_005269014.1:c.4024G>C XP_005269071.1:p.Val1342Leu
XM_006719493.1:c.4147G>C XP_006719556.1:p.Val1383Leu
XM_006719494.1:c.4075G>C XP_006719557.1:p.Val1359Leu
XM_006719496.1:c.4132G>C XP_006719559.1:p.Val1378Leu
XM_011538556.1:c.4138G>C XP_011536858.1:p.Val1380Leu
XM_005269007.3:c.4207G>C XP_005269064.1:p.Val1403Leu
XM_005269008.3:c.4192G>C XP_005269065.1:p.Val1398Leu
XM_005269009.3:c.4186G>C XP_005269066.1:p.Val1396Leu
XM_005269010.3:c.4168G>C XP_005269067.1:p.Val1390Leu
XM_005269011.3:c.4153G>C XP_005269068.1:p.Val1385Leu
XM_005269012.3:c.4078G>C XP_005269069.1:p.Val1360Leu
XM_005269013.3:c.4063G>C XP_005269070.1:p.Val1355Leu
XM_005269014.3:c.4024G>C XP_005269071.1:p.Val1342Leu
XM_006719493.3:c.4147G>C XP_006719556.1:p.Val1383Leu
XM_006719494.3:c.4075G>C XP_006719557.1:p.Val1359Leu
XM_011538556.3:c.4138G>C XP_011536858.1:p.Val1380Leu
XM_017019607.2:c.4153G>C XP_016875096.1:p.Val1385Leu
XM_017019608.2:c.4114G>C XP_016875097.1:p.Val1372Leu
XM_017019609.2:c.4003G>C XP_016875098.1:p.Val1335Leu
XM_017019610.2:c.4003G>C XP_016875099.1:p.Val1335Leu
XM_017019611.2:c.3985G>C XP_016875100.1:p.Val1329Leu
NM_001173463.2:c.4093G>C NP_001166934.1:p.Val1365Leu
NM_001173464.2:c.4204G>C MANE Select NP_001166935.1:p.Val1402Leu
NM_001173465.2:c.4045G>C NP_001166936.1:p.Val1349Leu
NM_017641.4:c.4165G>C NP_060111.2:p.Val1389Leu
NM_001378439.1:c.4207G>C NP_001365368.1:p.Val1403Leu
NM_001378440.1:c.4192G>C NP_001365369.1:p.Val1398Leu
NM_001378441.1:c.4168G>C NP_001365370.1:p.Val1390Leu