Canonical Allele Identifier: CA479233374

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703432C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309630C>T , CM000674.2:g.39309630C>T	GRCh38
NC_000012.11:g.39703432C>T , CM000674.1:g.39703432C>T	GRCh37
NC_000012.10:g.37989699C>T	NCBI36
NG_017067.1:g.138761G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4233G>A MANE Select	ENSP00000354878.5:p.Lys1411=
ENST00000636569.1:c.4170G>A	ENSP00000490369.1:p.Lys1390=
ENST00000361418.9:c.4233G>A	ENSP00000354878.5:p.Lys1411=
ENST00000361961.7:c.4194G>A	ENSP00000354851.3:p.Lys1398=
ENST00000541463.6:c.4074G>A	ENSP00000438075.2:p.Lys1358=
ENST00000544797.6:c.4122G>A	ENSP00000445606.2:p.Lys1374=
ENST00000547733.1:n.1547G>A
ENST00000551264.5:c.1176G>A	ENSP00000448792.1:p.Lys392=
ENST00000552961.5:c.2135G>A
NM_001173463.1:c.4122G>A	NP_001166934.1:p.Lys1374=
NM_001173464.1:c.4233G>A	NP_001166935.1:p.Lys1411=
NM_001173465.1:c.4074G>A	NP_001166936.1:p.Lys1358=
NM_017641.3:c.4194G>A	NP_060111.2:p.Lys1398=
XM_005269007.1:c.4236G>A	XP_005269064.1:p.Lys1412=
XM_005269008.1:c.4221G>A	XP_005269065.1:p.Lys1407=
XM_005269009.1:c.4215G>A	XP_005269066.1:p.Lys1405=
XM_005269010.1:c.4197G>A	XP_005269067.1:p.Lys1399=
XM_005269011.1:c.4182G>A	XP_005269068.1:p.Lys1394=
XM_005269012.1:c.4107G>A	XP_005269069.1:p.Lys1369=
XM_005269013.1:c.4092G>A	XP_005269070.1:p.Lys1364=
XM_005269014.1:c.4053G>A	XP_005269071.1:p.Lys1351=
XM_006719493.1:c.4176G>A	XP_006719556.1:p.Lys1392=
XM_006719494.1:c.4104G>A	XP_006719557.1:p.Lys1368=
XM_006719496.1:c.4161G>A	XP_006719559.1:p.Lys1387=
XM_011538556.1:c.4167G>A	XP_011536858.1:p.Lys1389=
XM_005269007.3:c.4236G>A	XP_005269064.1:p.Lys1412=
XM_005269008.3:c.4221G>A	XP_005269065.1:p.Lys1407=
XM_005269009.3:c.4215G>A	XP_005269066.1:p.Lys1405=
XM_005269010.3:c.4197G>A	XP_005269067.1:p.Lys1399=
XM_005269011.3:c.4182G>A	XP_005269068.1:p.Lys1394=
XM_005269012.3:c.4107G>A	XP_005269069.1:p.Lys1369=
XM_005269013.3:c.4092G>A	XP_005269070.1:p.Lys1364=
XM_005269014.3:c.4053G>A	XP_005269071.1:p.Lys1351=
XM_006719493.3:c.4176G>A	XP_006719556.1:p.Lys1392=
XM_006719494.3:c.4104G>A	XP_006719557.1:p.Lys1368=
XM_011538556.3:c.4167G>A	XP_011536858.1:p.Lys1389=
XM_017019607.2:c.4182G>A	XP_016875096.1:p.Lys1394=
XM_017019608.2:c.4143G>A	XP_016875097.1:p.Lys1381=
XM_017019609.2:c.4032G>A	XP_016875098.1:p.Lys1344=
XM_017019610.2:c.4032G>A	XP_016875099.1:p.Lys1344=
XM_017019611.2:c.4014G>A	XP_016875100.1:p.Lys1338=
NM_001173463.2:c.4122G>A	NP_001166934.1:p.Lys1374=
NM_001173464.2:c.4233G>A MANE Select	NP_001166935.1:p.Lys1411=
NM_001173465.2:c.4074G>A	NP_001166936.1:p.Lys1358=
NM_017641.4:c.4194G>A	NP_060111.2:p.Lys1398=
NM_001378439.1:c.4236G>A	NP_001365368.1:p.Lys1412=
NM_001378440.1:c.4221G>A	NP_001365369.1:p.Lys1407=
NM_001378441.1:c.4197G>A	NP_001365370.1:p.Lys1399=