Canonical Allele Identifier: CA6510185
Community Standard Title: NM_001173464.2(KIF21A):c.4388G>A (p.Gly1463Asp)
Gene: KIF21A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.39307619C>T , CM000674.2:g.39307619C>T GRCh38
NC_000012.11:g.39701421C>T , CM000674.1:g.39701421C>T GRCh37
NC_000012.10:g.37987688C>T NCBI36
NG_017067.1:g.140772G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001173464.2:c.4388G>A MANE Select NP_001166935.1:p.Gly1463Asp
ENST00000361418.10:c.4388G>A MANE Select ENSP00000354878.5:p.Gly1463Asp
NM_001173463.1:c.4277G>A NP_001166934.1:p.Gly1426Asp
NM_001173463.2:c.4277G>A NP_001166934.1:p.Gly1426Asp
NM_001173464.1:c.4388G>A NP_001166935.1:p.Gly1463Asp
NM_001173465.1:c.4229G>A NP_001166936.1:p.Gly1410Asp
NM_001173465.2:c.4229G>A NP_001166936.1:p.Gly1410Asp
NM_001378439.1:c.4391G>A NP_001365368.1:p.Gly1464Asp
NM_001378440.1:c.4376G>A NP_001365369.1:p.Gly1459Asp
NM_001378441.1:c.4352G>A NP_001365370.1:p.Gly1451Asp
NM_017641.3:c.4349G>A NP_060111.2:p.Gly1450Asp
NM_017641.4:c.4349G>A NP_060111.2:p.Gly1450Asp
ENST00000361418.9:c.4388G>A ENSP00000354878.5:p.Gly1463Asp
ENST00000361961.7:c.4349G>A ENSP00000354851.3:p.Gly1450Asp
ENST00000541463.6:c.4229G>A ENSP00000438075.2:p.Gly1410Asp
ENST00000544797.6:c.4277G>A ENSP00000445606.2:p.Gly1426Asp
ENST00000547733.1:n.1702G>A
ENST00000551264.5:c.1331G>A ENSP00000448792.1:p.Gly444Asp
ENST00000552961.5:c.2290G>A
ENST00000636569.1:c.4325G>A ENSP00000490369.1:p.Gly1442Asp
XM_005269007.1:c.4391G>A XP_005269064.1:p.Gly1464Asp
XM_005269007.3:c.4391G>A XP_005269064.1:p.Gly1464Asp
XM_005269008.1:c.4376G>A XP_005269065.1:p.Gly1459Asp
XM_005269008.3:c.4376G>A XP_005269065.1:p.Gly1459Asp
XM_005269009.1:c.4370G>A XP_005269066.1:p.Gly1457Asp
XM_005269009.3:c.4370G>A XP_005269066.1:p.Gly1457Asp
XM_005269010.1:c.4352G>A XP_005269067.1:p.Gly1451Asp
XM_005269010.3:c.4352G>A XP_005269067.1:p.Gly1451Asp
XM_005269011.1:c.4337G>A XP_005269068.1:p.Gly1446Asp
XM_005269011.3:c.4337G>A XP_005269068.1:p.Gly1446Asp
XM_005269012.1:c.4262G>A XP_005269069.1:p.Gly1421Asp
XM_005269012.3:c.4262G>A XP_005269069.1:p.Gly1421Asp
XM_005269013.1:c.4247G>A XP_005269070.1:p.Gly1416Asp
XM_005269013.3:c.4247G>A XP_005269070.1:p.Gly1416Asp
XM_005269014.1:c.4208G>A XP_005269071.1:p.Gly1403Asp
XM_005269014.3:c.4208G>A XP_005269071.1:p.Gly1403Asp
XM_006719493.1:c.4331G>A XP_006719556.1:p.Gly1444Asp
XM_006719493.3:c.4331G>A XP_006719556.1:p.Gly1444Asp
XM_006719494.1:c.4259G>A XP_006719557.1:p.Gly1420Asp
XM_006719494.3:c.4259G>A XP_006719557.1:p.Gly1420Asp
XM_006719496.1:c.4316G>A XP_006719559.1:p.Gly1439Asp
XM_011538556.1:c.4322G>A XP_011536858.1:p.Gly1441Asp
XM_011538556.3:c.4322G>A XP_011536858.1:p.Gly1441Asp
XM_017019607.2:c.4337G>A XP_016875096.1:p.Gly1446Asp
XM_017019608.2:c.4298G>A XP_016875097.1:p.Gly1433Asp
XM_017019609.2:c.4187G>A XP_016875098.1:p.Gly1396Asp
XM_017019610.2:c.4187G>A XP_016875099.1:p.Gly1396Asp
XM_017019611.2:c.4169G>A XP_016875100.1:p.Gly1390Asp