Canonical Allele Identifier: CA479233383

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703444T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309642T>G , CM000674.2:g.39309642T>G	GRCh38
NC_000012.11:g.39703444T>G , CM000674.1:g.39703444T>G	GRCh37
NC_000012.10:g.37989711T>G	NCBI36
NG_017067.1:g.138749A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4221A>C MANE Select	ENSP00000354878.5:p.Thr1407=
ENST00000636569.1:c.4158A>C	ENSP00000490369.1:p.Thr1386=
ENST00000361418.9:c.4221A>C	ENSP00000354878.5:p.Thr1407=
ENST00000361961.7:c.4182A>C	ENSP00000354851.3:p.Thr1394=
ENST00000541463.6:c.4062A>C	ENSP00000438075.2:p.Thr1354=
ENST00000544797.6:c.4110A>C	ENSP00000445606.2:p.Thr1370=
ENST00000547733.1:n.1535A>C
ENST00000551264.5:c.1164A>C	ENSP00000448792.1:p.Thr388=
ENST00000552961.5:c.2123A>C
NM_001173463.1:c.4110A>C	NP_001166934.1:p.Thr1370=
NM_001173464.1:c.4221A>C	NP_001166935.1:p.Thr1407=
NM_001173465.1:c.4062A>C	NP_001166936.1:p.Thr1354=
NM_017641.3:c.4182A>C	NP_060111.2:p.Thr1394=
XM_005269007.1:c.4224A>C	XP_005269064.1:p.Thr1408=
XM_005269008.1:c.4209A>C	XP_005269065.1:p.Thr1403=
XM_005269009.1:c.4203A>C	XP_005269066.1:p.Thr1401=
XM_005269010.1:c.4185A>C	XP_005269067.1:p.Thr1395=
XM_005269011.1:c.4170A>C	XP_005269068.1:p.Thr1390=
XM_005269012.1:c.4095A>C	XP_005269069.1:p.Thr1365=
XM_005269013.1:c.4080A>C	XP_005269070.1:p.Thr1360=
XM_005269014.1:c.4041A>C	XP_005269071.1:p.Thr1347=
XM_006719493.1:c.4164A>C	XP_006719556.1:p.Thr1388=
XM_006719494.1:c.4092A>C	XP_006719557.1:p.Thr1364=
XM_006719496.1:c.4149A>C	XP_006719559.1:p.Thr1383=
XM_011538556.1:c.4155A>C	XP_011536858.1:p.Thr1385=
XM_005269007.3:c.4224A>C	XP_005269064.1:p.Thr1408=
XM_005269008.3:c.4209A>C	XP_005269065.1:p.Thr1403=
XM_005269009.3:c.4203A>C	XP_005269066.1:p.Thr1401=
XM_005269010.3:c.4185A>C	XP_005269067.1:p.Thr1395=
XM_005269011.3:c.4170A>C	XP_005269068.1:p.Thr1390=
XM_005269012.3:c.4095A>C	XP_005269069.1:p.Thr1365=
XM_005269013.3:c.4080A>C	XP_005269070.1:p.Thr1360=
XM_005269014.3:c.4041A>C	XP_005269071.1:p.Thr1347=
XM_006719493.3:c.4164A>C	XP_006719556.1:p.Thr1388=
XM_006719494.3:c.4092A>C	XP_006719557.1:p.Thr1364=
XM_011538556.3:c.4155A>C	XP_011536858.1:p.Thr1385=
XM_017019607.2:c.4170A>C	XP_016875096.1:p.Thr1390=
XM_017019608.2:c.4131A>C	XP_016875097.1:p.Thr1377=
XM_017019609.2:c.4020A>C	XP_016875098.1:p.Thr1340=
XM_017019610.2:c.4020A>C	XP_016875099.1:p.Thr1340=
XM_017019611.2:c.4002A>C	XP_016875100.1:p.Thr1334=
NM_001173463.2:c.4110A>C	NP_001166934.1:p.Thr1370=
NM_001173464.2:c.4221A>C MANE Select	NP_001166935.1:p.Thr1407=
NM_001173465.2:c.4062A>C	NP_001166936.1:p.Thr1354=
NM_017641.4:c.4182A>C	NP_060111.2:p.Thr1394=
NM_001378439.1:c.4224A>C	NP_001365368.1:p.Thr1408=
NM_001378440.1:c.4209A>C	NP_001365369.1:p.Thr1403=
NM_001378441.1:c.4185A>C	NP_001365370.1:p.Thr1395=