Canonical Allele Identifier: CA6510156
Community Standard Title: NM_001173464.2(KIF21A):c.4515T>G (p.Ser1505Arg)
Gene: KIF21A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.39304866A>C , CM000674.2:g.39304866A>C GRCh38
NC_000012.11:g.39698668A>C , CM000674.1:g.39698668A>C GRCh37
NC_000012.10:g.37984935A>C NCBI36
NG_017067.1:g.143525T>G

Transcript Alleles

HGVS Amino-acid Change
NM_001173464.2:c.4515T>G MANE Select NP_001166935.1:p.Ser1505Arg
ENST00000361418.10:c.4515T>G MANE Select ENSP00000354878.5:p.Ser1505Arg
NM_001173463.1:c.4404T>G NP_001166934.1:p.Ser1468Arg
NM_001173463.2:c.4404T>G NP_001166934.1:p.Ser1468Arg
NM_001173464.1:c.4515T>G NP_001166935.1:p.Ser1505Arg
NM_001173465.1:c.4356T>G NP_001166936.1:p.Ser1452Arg
NM_001173465.2:c.4356T>G NP_001166936.1:p.Ser1452Arg
NM_001378439.1:c.4518T>G NP_001365368.1:p.Ser1506Arg
NM_001378440.1:c.4503T>G NP_001365369.1:p.Ser1501Arg
NM_001378441.1:c.4479T>G NP_001365370.1:p.Ser1493Arg
NM_017641.3:c.4476T>G NP_060111.2:p.Ser1492Arg
NM_017641.4:c.4476T>G NP_060111.2:p.Ser1492Arg
ENST00000361418.9:c.4515T>G ENSP00000354878.5:p.Ser1505Arg
ENST00000361961.7:c.4476T>G ENSP00000354851.3:p.Ser1492Arg
ENST00000541463.6:c.4356T>G ENSP00000438075.2:p.Ser1452Arg
ENST00000544797.6:c.4404T>G ENSP00000445606.2:p.Ser1468Arg
ENST00000547733.1:n.1829T>G
ENST00000551264.5:c.1458T>G ENSP00000448792.1:p.Ser486Arg
ENST00000552961.5:c.2417T>G
ENST00000636569.1:c.4452T>G ENSP00000490369.1:p.Ser1484Arg
XM_005269007.1:c.4518T>G XP_005269064.1:p.Ser1506Arg
XM_005269007.3:c.4518T>G XP_005269064.1:p.Ser1506Arg
XM_005269008.1:c.4503T>G XP_005269065.1:p.Ser1501Arg
XM_005269008.3:c.4503T>G XP_005269065.1:p.Ser1501Arg
XM_005269009.1:c.4497T>G XP_005269066.1:p.Ser1499Arg
XM_005269009.3:c.4497T>G XP_005269066.1:p.Ser1499Arg
XM_005269010.1:c.4479T>G XP_005269067.1:p.Ser1493Arg
XM_005269010.3:c.4479T>G XP_005269067.1:p.Ser1493Arg
XM_005269011.1:c.4464T>G XP_005269068.1:p.Ser1488Arg
XM_005269011.3:c.4464T>G XP_005269068.1:p.Ser1488Arg
XM_005269012.1:c.4389T>G XP_005269069.1:p.Ser1463Arg
XM_005269012.3:c.4389T>G XP_005269069.1:p.Ser1463Arg
XM_005269013.1:c.4374T>G XP_005269070.1:p.Ser1458Arg
XM_005269013.3:c.4374T>G XP_005269070.1:p.Ser1458Arg
XM_005269014.1:c.4335T>G XP_005269071.1:p.Ser1445Arg
XM_005269014.3:c.4335T>G XP_005269071.1:p.Ser1445Arg
XM_006719493.1:c.4458T>G XP_006719556.1:p.Ser1486Arg
XM_006719493.3:c.4458T>G XP_006719556.1:p.Ser1486Arg
XM_006719494.1:c.4386T>G XP_006719557.1:p.Ser1462Arg
XM_006719494.3:c.4386T>G XP_006719557.1:p.Ser1462Arg
XM_006719496.1:c.4443T>G XP_006719559.1:p.Ser1481Arg
XM_011538556.1:c.4449T>G XP_011536858.1:p.Ser1483Arg
XM_011538556.3:c.4449T>G XP_011536858.1:p.Ser1483Arg
XM_017019607.2:c.4464T>G XP_016875096.1:p.Ser1488Arg
XM_017019608.2:c.4425T>G XP_016875097.1:p.Ser1475Arg
XM_017019609.2:c.4314T>G XP_016875098.1:p.Ser1438Arg
XM_017019610.2:c.4314T>G XP_016875099.1:p.Ser1438Arg
XM_017019611.2:c.4296T>G XP_016875100.1:p.Ser1432Arg