Canonical Allele Identifier: CA384386905

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703419T>A (hg19) ; chr12:g.39309617T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309617T>A , CM000674.2:g.39309617T>A	GRCh38
NC_000012.11:g.39703419T>A , CM000674.1:g.39703419T>A	GRCh37
NC_000012.10:g.37989686T>A	NCBI36
NG_017067.1:g.138774A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4246A>T MANE Select	ENSP00000354878.5:p.Arg1416Ter
ENST00000636569.1:c.4183A>T	ENSP00000490369.1:p.Arg1395Ter
ENST00000361418.9:c.4246A>T	ENSP00000354878.5:p.Arg1416Ter
ENST00000361961.7:c.4207A>T	ENSP00000354851.3:p.Arg1403Ter
ENST00000541463.6:c.4087A>T	ENSP00000438075.2:p.Arg1363Ter
ENST00000544797.6:c.4135A>T	ENSP00000445606.2:p.Arg1379Ter
ENST00000547733.1:n.1560A>T
ENST00000551264.5:c.1189A>T	ENSP00000448792.1:p.Arg397Ter
ENST00000552961.5:c.2148A>T
NM_001173463.1:c.4135A>T	NP_001166934.1:p.Arg1379Ter
NM_001173464.1:c.4246A>T	NP_001166935.1:p.Arg1416Ter
NM_001173465.1:c.4087A>T	NP_001166936.1:p.Arg1363Ter
NM_017641.3:c.4207A>T	NP_060111.2:p.Arg1403Ter
XM_005269007.1:c.4249A>T	XP_005269064.1:p.Arg1417Ter
XM_005269008.1:c.4234A>T	XP_005269065.1:p.Arg1412Ter
XM_005269009.1:c.4228A>T	XP_005269066.1:p.Arg1410Ter
XM_005269010.1:c.4210A>T	XP_005269067.1:p.Arg1404Ter
XM_005269011.1:c.4195A>T	XP_005269068.1:p.Arg1399Ter
XM_005269012.1:c.4120A>T	XP_005269069.1:p.Arg1374Ter
XM_005269013.1:c.4105A>T	XP_005269070.1:p.Arg1369Ter
XM_005269014.1:c.4066A>T	XP_005269071.1:p.Arg1356Ter
XM_006719493.1:c.4189A>T	XP_006719556.1:p.Arg1397Ter
XM_006719494.1:c.4117A>T	XP_006719557.1:p.Arg1373Ter
XM_006719496.1:c.4174A>T	XP_006719559.1:p.Arg1392Ter
XM_011538556.1:c.4180A>T	XP_011536858.1:p.Arg1394Ter
XM_005269007.3:c.4249A>T	XP_005269064.1:p.Arg1417Ter
XM_005269008.3:c.4234A>T	XP_005269065.1:p.Arg1412Ter
XM_005269009.3:c.4228A>T	XP_005269066.1:p.Arg1410Ter
XM_005269010.3:c.4210A>T	XP_005269067.1:p.Arg1404Ter
XM_005269011.3:c.4195A>T	XP_005269068.1:p.Arg1399Ter
XM_005269012.3:c.4120A>T	XP_005269069.1:p.Arg1374Ter
XM_005269013.3:c.4105A>T	XP_005269070.1:p.Arg1369Ter
XM_005269014.3:c.4066A>T	XP_005269071.1:p.Arg1356Ter
XM_006719493.3:c.4189A>T	XP_006719556.1:p.Arg1397Ter
XM_006719494.3:c.4117A>T	XP_006719557.1:p.Arg1373Ter
XM_011538556.3:c.4180A>T	XP_011536858.1:p.Arg1394Ter
XM_017019607.2:c.4195A>T	XP_016875096.1:p.Arg1399Ter
XM_017019608.2:c.4156A>T	XP_016875097.1:p.Arg1386Ter
XM_017019609.2:c.4045A>T	XP_016875098.1:p.Arg1349Ter
XM_017019610.2:c.4045A>T	XP_016875099.1:p.Arg1349Ter
XM_017019611.2:c.4027A>T	XP_016875100.1:p.Arg1343Ter
NM_001173463.2:c.4135A>T	NP_001166934.1:p.Arg1379Ter
NM_001173464.2:c.4246A>T MANE Select	NP_001166935.1:p.Arg1416Ter
NM_001173465.2:c.4087A>T	NP_001166936.1:p.Arg1363Ter
NM_017641.4:c.4207A>T	NP_060111.2:p.Arg1403Ter
NM_001378439.1:c.4249A>T	NP_001365368.1:p.Arg1417Ter
NM_001378440.1:c.4234A>T	NP_001365369.1:p.Arg1412Ter
NM_001378441.1:c.4210A>T	NP_001365370.1:p.Arg1404Ter