Canonical Allele Identifier: CA479233392

Gene: KIF21A

Linked Data

• dbSNP Id: rs2137324634
• MyVariant Identifiers: chr12:g.39703453A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309651A>T , CM000674.2:g.39309651A>T	GRCh38
NC_000012.11:g.39703453A>T , CM000674.1:g.39703453A>T	GRCh37
NC_000012.10:g.37989720A>T	NCBI36
NG_017067.1:g.138740T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4212T>A MANE Select	ENSP00000354878.5:p.Thr1404=
ENST00000636569.1:c.4149T>A	ENSP00000490369.1:p.Thr1383=
ENST00000361418.9:c.4212T>A	ENSP00000354878.5:p.Thr1404=
ENST00000361961.7:c.4173T>A	ENSP00000354851.3:p.Thr1391=
ENST00000541463.6:c.4053T>A	ENSP00000438075.2:p.Thr1351=
ENST00000544797.6:c.4101T>A	ENSP00000445606.2:p.Thr1367=
ENST00000547733.1:n.1526T>A
ENST00000551264.5:c.1155T>A	ENSP00000448792.1:p.Thr385=
ENST00000552961.5:c.2114T>A
NM_001173463.1:c.4101T>A	NP_001166934.1:p.Thr1367=
NM_001173464.1:c.4212T>A	NP_001166935.1:p.Thr1404=
NM_001173465.1:c.4053T>A	NP_001166936.1:p.Thr1351=
NM_017641.3:c.4173T>A	NP_060111.2:p.Thr1391=
XM_005269007.1:c.4215T>A	XP_005269064.1:p.Thr1405=
XM_005269008.1:c.4200T>A	XP_005269065.1:p.Thr1400=
XM_005269009.1:c.4194T>A	XP_005269066.1:p.Thr1398=
XM_005269010.1:c.4176T>A	XP_005269067.1:p.Thr1392=
XM_005269011.1:c.4161T>A	XP_005269068.1:p.Thr1387=
XM_005269012.1:c.4086T>A	XP_005269069.1:p.Thr1362=
XM_005269013.1:c.4071T>A	XP_005269070.1:p.Thr1357=
XM_005269014.1:c.4032T>A	XP_005269071.1:p.Thr1344=
XM_006719493.1:c.4155T>A	XP_006719556.1:p.Thr1385=
XM_006719494.1:c.4083T>A	XP_006719557.1:p.Thr1361=
XM_006719496.1:c.4140T>A	XP_006719559.1:p.Thr1380=
XM_011538556.1:c.4146T>A	XP_011536858.1:p.Thr1382=
XM_005269007.3:c.4215T>A	XP_005269064.1:p.Thr1405=
XM_005269008.3:c.4200T>A	XP_005269065.1:p.Thr1400=
XM_005269009.3:c.4194T>A	XP_005269066.1:p.Thr1398=
XM_005269010.3:c.4176T>A	XP_005269067.1:p.Thr1392=
XM_005269011.3:c.4161T>A	XP_005269068.1:p.Thr1387=
XM_005269012.3:c.4086T>A	XP_005269069.1:p.Thr1362=
XM_005269013.3:c.4071T>A	XP_005269070.1:p.Thr1357=
XM_005269014.3:c.4032T>A	XP_005269071.1:p.Thr1344=
XM_006719493.3:c.4155T>A	XP_006719556.1:p.Thr1385=
XM_006719494.3:c.4083T>A	XP_006719557.1:p.Thr1361=
XM_011538556.3:c.4146T>A	XP_011536858.1:p.Thr1382=
XM_017019607.2:c.4161T>A	XP_016875096.1:p.Thr1387=
XM_017019608.2:c.4122T>A	XP_016875097.1:p.Thr1374=
XM_017019609.2:c.4011T>A	XP_016875098.1:p.Thr1337=
XM_017019610.2:c.4011T>A	XP_016875099.1:p.Thr1337=
XM_017019611.2:c.3993T>A	XP_016875100.1:p.Thr1331=
NM_001173463.2:c.4101T>A	NP_001166934.1:p.Thr1367=
NM_001173464.2:c.4212T>A MANE Select	NP_001166935.1:p.Thr1404=
NM_001173465.2:c.4053T>A	NP_001166936.1:p.Thr1351=
NM_017641.4:c.4173T>A	NP_060111.2:p.Thr1391=
NM_001378439.1:c.4215T>A	NP_001365368.1:p.Thr1405=
NM_001378440.1:c.4200T>A	NP_001365369.1:p.Thr1400=
NM_001378441.1:c.4176T>A	NP_001365370.1:p.Thr1392=