Canonical Allele Identifier: CA479233343

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703390T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309588T>A , CM000674.2:g.39309588T>A	GRCh38
NC_000012.11:g.39703390T>A , CM000674.1:g.39703390T>A	GRCh37
NC_000012.10:g.37989657T>A	NCBI36
NG_017067.1:g.138803A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000361418.10:c.4275A>T MANE Select	ENSP00000354878.5:p.Leu1425=
ENST00000636569.1:c.4212A>T	ENSP00000490369.1:p.Leu1404=
ENST00000361418.9:c.4275A>T	ENSP00000354878.5:p.Leu1425=
ENST00000361961.7:c.4236A>T	ENSP00000354851.3:p.Leu1412=
ENST00000541463.6:c.4116A>T	ENSP00000438075.2:p.Leu1372=
ENST00000544797.6:c.4164A>T	ENSP00000445606.2:p.Leu1388=
ENST00000547733.1:n.1589A>T
ENST00000551264.5:c.1218A>T	ENSP00000448792.1:p.Leu406=
ENST00000552961.5:c.2177A>T
NM_001173463.1:c.4164A>T	NP_001166934.1:p.Leu1388=
NM_001173464.1:c.4275A>T	NP_001166935.1:p.Leu1425=
NM_001173465.1:c.4116A>T	NP_001166936.1:p.Leu1372=
NM_017641.3:c.4236A>T	NP_060111.2:p.Leu1412=
XM_005269007.1:c.4278A>T	XP_005269064.1:p.Leu1426=
XM_005269008.1:c.4263A>T	XP_005269065.1:p.Leu1421=
XM_005269009.1:c.4257A>T	XP_005269066.1:p.Leu1419=
XM_005269010.1:c.4239A>T	XP_005269067.1:p.Leu1413=
XM_005269011.1:c.4224A>T	XP_005269068.1:p.Leu1408=
XM_005269012.1:c.4149A>T	XP_005269069.1:p.Leu1383=
XM_005269013.1:c.4134A>T	XP_005269070.1:p.Leu1378=
XM_005269014.1:c.4095A>T	XP_005269071.1:p.Leu1365=
XM_006719493.1:c.4218A>T	XP_006719556.1:p.Leu1406=
XM_006719494.1:c.4146A>T	XP_006719557.1:p.Leu1382=
XM_006719496.1:c.4203A>T	XP_006719559.1:p.Leu1401=
XM_011538556.1:c.4209A>T	XP_011536858.1:p.Leu1403=
XM_005269007.3:c.4278A>T	XP_005269064.1:p.Leu1426=
XM_005269008.3:c.4263A>T	XP_005269065.1:p.Leu1421=
XM_005269009.3:c.4257A>T	XP_005269066.1:p.Leu1419=
XM_005269010.3:c.4239A>T	XP_005269067.1:p.Leu1413=
XM_005269011.3:c.4224A>T	XP_005269068.1:p.Leu1408=
XM_005269012.3:c.4149A>T	XP_005269069.1:p.Leu1383=
XM_005269013.3:c.4134A>T	XP_005269070.1:p.Leu1378=
XM_005269014.3:c.4095A>T	XP_005269071.1:p.Leu1365=
XM_006719493.3:c.4218A>T	XP_006719556.1:p.Leu1406=
XM_006719494.3:c.4146A>T	XP_006719557.1:p.Leu1382=
XM_011538556.3:c.4209A>T	XP_011536858.1:p.Leu1403=
XM_017019607.2:c.4224A>T	XP_016875096.1:p.Leu1408=
XM_017019608.2:c.4185A>T	XP_016875097.1:p.Leu1395=
XM_017019609.2:c.4074A>T	XP_016875098.1:p.Leu1358=
XM_017019610.2:c.4074A>T	XP_016875099.1:p.Leu1358=
XM_017019611.2:c.4056A>T	XP_016875100.1:p.Leu1352=
NM_001173463.2:c.4164A>T	NP_001166934.1:p.Leu1388=
NM_001173464.2:c.4275A>T MANE Select	NP_001166935.1:p.Leu1425=
NM_001173465.2:c.4116A>T	NP_001166936.1:p.Leu1372=
NM_017641.4:c.4236A>T	NP_060111.2:p.Leu1412=
NM_001378439.1:c.4278A>T	NP_001365368.1:p.Leu1426=
NM_001378440.1:c.4263A>T	NP_001365369.1:p.Leu1421=
NM_001378441.1:c.4239A>T	NP_001365370.1:p.Leu1413=