Canonical Allele Identifier: CA384387391

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703494C>A (hg19) ; chr12:g.39309692C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309692C>A , CM000674.2:g.39309692C>A	GRCh38
NC_000012.11:g.39703494C>A , CM000674.1:g.39703494C>A	GRCh37
NC_000012.10:g.37989761C>A	NCBI36
NG_017067.1:g.138699G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4171G>T MANE Select	ENSP00000354878.5:p.Val1391Leu
ENST00000636569.1:c.4108G>T	ENSP00000490369.1:p.Val1370Leu
ENST00000361418.9:c.4171G>T	ENSP00000354878.5:p.Val1391Leu
ENST00000361961.7:c.4132G>T	ENSP00000354851.3:p.Val1378Leu
ENST00000541463.6:c.4012G>T	ENSP00000438075.2:p.Val1338Leu
ENST00000544797.6:c.4060G>T	ENSP00000445606.2:p.Val1354Leu
ENST00000547733.1:n.1485G>T
ENST00000551264.5:c.1114G>T	ENSP00000448792.1:p.Val372Leu
ENST00000552961.5:c.2073G>T
NM_001173463.1:c.4060G>T	NP_001166934.1:p.Val1354Leu
NM_001173464.1:c.4171G>T	NP_001166935.1:p.Val1391Leu
NM_001173465.1:c.4012G>T	NP_001166936.1:p.Val1338Leu
NM_017641.3:c.4132G>T	NP_060111.2:p.Val1378Leu
XM_005269007.1:c.4174G>T	XP_005269064.1:p.Val1392Leu
XM_005269008.1:c.4159G>T	XP_005269065.1:p.Val1387Leu
XM_005269009.1:c.4153G>T	XP_005269066.1:p.Val1385Leu
XM_005269010.1:c.4135G>T	XP_005269067.1:p.Val1379Leu
XM_005269011.1:c.4120G>T	XP_005269068.1:p.Val1374Leu
XM_005269012.1:c.4045G>T	XP_005269069.1:p.Val1349Leu
XM_005269013.1:c.4030G>T	XP_005269070.1:p.Val1344Leu
XM_005269014.1:c.3991G>T	XP_005269071.1:p.Val1331Leu
XM_006719493.1:c.4114G>T	XP_006719556.1:p.Val1372Leu
XM_006719494.1:c.4042G>T	XP_006719557.1:p.Val1348Leu
XM_006719496.1:c.4099G>T	XP_006719559.1:p.Val1367Leu
XM_011538556.1:c.4105G>T	XP_011536858.1:p.Val1369Leu
XM_005269007.3:c.4174G>T	XP_005269064.1:p.Val1392Leu
XM_005269008.3:c.4159G>T	XP_005269065.1:p.Val1387Leu
XM_005269009.3:c.4153G>T	XP_005269066.1:p.Val1385Leu
XM_005269010.3:c.4135G>T	XP_005269067.1:p.Val1379Leu
XM_005269011.3:c.4120G>T	XP_005269068.1:p.Val1374Leu
XM_005269012.3:c.4045G>T	XP_005269069.1:p.Val1349Leu
XM_005269013.3:c.4030G>T	XP_005269070.1:p.Val1344Leu
XM_005269014.3:c.3991G>T	XP_005269071.1:p.Val1331Leu
XM_006719493.3:c.4114G>T	XP_006719556.1:p.Val1372Leu
XM_006719494.3:c.4042G>T	XP_006719557.1:p.Val1348Leu
XM_011538556.3:c.4105G>T	XP_011536858.1:p.Val1369Leu
XM_017019607.2:c.4120G>T	XP_016875096.1:p.Val1374Leu
XM_017019608.2:c.4081G>T	XP_016875097.1:p.Val1361Leu
XM_017019609.2:c.3970G>T	XP_016875098.1:p.Val1324Leu
XM_017019610.2:c.3970G>T	XP_016875099.1:p.Val1324Leu
XM_017019611.2:c.3952G>T	XP_016875100.1:p.Val1318Leu
NM_001173463.2:c.4060G>T	NP_001166934.1:p.Val1354Leu
NM_001173464.2:c.4171G>T MANE Select	NP_001166935.1:p.Val1391Leu
NM_001173465.2:c.4012G>T	NP_001166936.1:p.Val1338Leu
NM_017641.4:c.4132G>T	NP_060111.2:p.Val1378Leu
NM_001378439.1:c.4174G>T	NP_001365368.1:p.Val1392Leu
NM_001378440.1:c.4159G>T	NP_001365369.1:p.Val1387Leu
NM_001378441.1:c.4135G>T	NP_001365370.1:p.Val1379Leu