Canonical Allele Identifier: CA384387310

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703481T>A (hg19) ; chr12:g.39309679T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309679T>A , CM000674.2:g.39309679T>A	GRCh38
NC_000012.11:g.39703481T>A , CM000674.1:g.39703481T>A	GRCh37
NC_000012.10:g.37989748T>A	NCBI36
NG_017067.1:g.138712A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4184A>T MANE Select	ENSP00000354878.5:p.Tyr1395Phe
ENST00000636569.1:c.4121A>T	ENSP00000490369.1:p.Tyr1374Phe
ENST00000361418.9:c.4184A>T	ENSP00000354878.5:p.Tyr1395Phe
ENST00000361961.7:c.4145A>T	ENSP00000354851.3:p.Tyr1382Phe
ENST00000541463.6:c.4025A>T	ENSP00000438075.2:p.Tyr1342Phe
ENST00000544797.6:c.4073A>T	ENSP00000445606.2:p.Tyr1358Phe
ENST00000547733.1:n.1498A>T
ENST00000551264.5:c.1127A>T	ENSP00000448792.1:p.Tyr376Phe
ENST00000552961.5:c.2086A>T
NM_001173463.1:c.4073A>T	NP_001166934.1:p.Tyr1358Phe
NM_001173464.1:c.4184A>T	NP_001166935.1:p.Tyr1395Phe
NM_001173465.1:c.4025A>T	NP_001166936.1:p.Tyr1342Phe
NM_017641.3:c.4145A>T	NP_060111.2:p.Tyr1382Phe
XM_005269007.1:c.4187A>T	XP_005269064.1:p.Tyr1396Phe
XM_005269008.1:c.4172A>T	XP_005269065.1:p.Tyr1391Phe
XM_005269009.1:c.4166A>T	XP_005269066.1:p.Tyr1389Phe
XM_005269010.1:c.4148A>T	XP_005269067.1:p.Tyr1383Phe
XM_005269011.1:c.4133A>T	XP_005269068.1:p.Tyr1378Phe
XM_005269012.1:c.4058A>T	XP_005269069.1:p.Tyr1353Phe
XM_005269013.1:c.4043A>T	XP_005269070.1:p.Tyr1348Phe
XM_005269014.1:c.4004A>T	XP_005269071.1:p.Tyr1335Phe
XM_006719493.1:c.4127A>T	XP_006719556.1:p.Tyr1376Phe
XM_006719494.1:c.4055A>T	XP_006719557.1:p.Tyr1352Phe
XM_006719496.1:c.4112A>T	XP_006719559.1:p.Tyr1371Phe
XM_011538556.1:c.4118A>T	XP_011536858.1:p.Tyr1373Phe
XM_005269007.3:c.4187A>T	XP_005269064.1:p.Tyr1396Phe
XM_005269008.3:c.4172A>T	XP_005269065.1:p.Tyr1391Phe
XM_005269009.3:c.4166A>T	XP_005269066.1:p.Tyr1389Phe
XM_005269010.3:c.4148A>T	XP_005269067.1:p.Tyr1383Phe
XM_005269011.3:c.4133A>T	XP_005269068.1:p.Tyr1378Phe
XM_005269012.3:c.4058A>T	XP_005269069.1:p.Tyr1353Phe
XM_005269013.3:c.4043A>T	XP_005269070.1:p.Tyr1348Phe
XM_005269014.3:c.4004A>T	XP_005269071.1:p.Tyr1335Phe
XM_006719493.3:c.4127A>T	XP_006719556.1:p.Tyr1376Phe
XM_006719494.3:c.4055A>T	XP_006719557.1:p.Tyr1352Phe
XM_011538556.3:c.4118A>T	XP_011536858.1:p.Tyr1373Phe
XM_017019607.2:c.4133A>T	XP_016875096.1:p.Tyr1378Phe
XM_017019608.2:c.4094A>T	XP_016875097.1:p.Tyr1365Phe
XM_017019609.2:c.3983A>T	XP_016875098.1:p.Tyr1328Phe
XM_017019610.2:c.3983A>T	XP_016875099.1:p.Tyr1328Phe
XM_017019611.2:c.3965A>T	XP_016875100.1:p.Tyr1322Phe
NM_001173463.2:c.4073A>T	NP_001166934.1:p.Tyr1358Phe
NM_001173464.2:c.4184A>T MANE Select	NP_001166935.1:p.Tyr1395Phe
NM_001173465.2:c.4025A>T	NP_001166936.1:p.Tyr1342Phe
NM_017641.4:c.4145A>T	NP_060111.2:p.Tyr1382Phe
NM_001378439.1:c.4187A>T	NP_001365368.1:p.Tyr1396Phe
NM_001378440.1:c.4172A>T	NP_001365369.1:p.Tyr1391Phe
NM_001378441.1:c.4148A>T	NP_001365370.1:p.Tyr1383Phe