Canonical Allele Identifier: CA2618258888

Gene: KIF21A

Linked Data

• gnomAD v4: 12-39309586-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309588del , CM000674.2:g.39309588del	GRCh38
NC_000012.11:g.39703390del , CM000674.1:g.39703390del	GRCh37
NC_000012.10:g.37989657del	NCBI36
NG_017067.1:g.138804del

Transcript Alleles

HGVS	Amino-acid change
ENST00000361418.10:c.4276del MANE Select	ENSP00000354878.5:p.Thr1426ArgfsTer20
ENST00000636569.1:c.4213del	ENSP00000490369.1:p.Thr1405ArgfsTer20
ENST00000361418.9:c.4276del	ENSP00000354878.5:p.Thr1426ArgfsTer20
ENST00000361961.7:c.4237del	ENSP00000354851.3:p.Thr1413ArgfsTer20
ENST00000541463.6:c.4117del	ENSP00000438075.2:p.Thr1373ArgfsTer20
ENST00000544797.6:c.4165del	ENSP00000445606.2:p.Thr1389ArgfsTer20
ENST00000547733.1:n.1590del
ENST00000551264.5:c.1219del	ENSP00000448792.1:p.Thr407ArgfsTer20
ENST00000552961.5:c.2178del
NM_001173463.1:c.4165del	NP_001166934.1:p.Thr1389ArgfsTer20
NM_001173464.1:c.4276del	NP_001166935.1:p.Thr1426ArgfsTer20
NM_001173465.1:c.4117del	NP_001166936.1:p.Thr1373ArgfsTer20
NM_017641.3:c.4237del	NP_060111.2:p.Thr1413ArgfsTer20
XM_005269007.1:c.4279del	XP_005269064.1:p.Thr1427ArgfsTer20
XM_005269008.1:c.4264del	XP_005269065.1:p.Thr1422ArgfsTer20
XM_005269009.1:c.4258del	XP_005269066.1:p.Thr1420ArgfsTer20
XM_005269010.1:c.4240del	XP_005269067.1:p.Thr1414ArgfsTer20
XM_005269011.1:c.4225del	XP_005269068.1:p.Thr1409ArgfsTer20
XM_005269012.1:c.4150del	XP_005269069.1:p.Thr1384ArgfsTer20
XM_005269013.1:c.4135del	XP_005269070.1:p.Thr1379ArgfsTer20
XM_005269014.1:c.4096del	XP_005269071.1:p.Thr1366ArgfsTer20
XM_006719493.1:c.4219del	XP_006719556.1:p.Thr1407ArgfsTer20
XM_006719494.1:c.4147del	XP_006719557.1:p.Thr1383ArgfsTer20
XM_006719496.1:c.4204del	XP_006719559.1:p.Thr1402ArgfsTer20
XM_011538556.1:c.4210del	XP_011536858.1:p.Thr1404ArgfsTer20
XM_005269007.3:c.4279del	XP_005269064.1:p.Thr1427ArgfsTer20
XM_005269008.3:c.4264del	XP_005269065.1:p.Thr1422ArgfsTer20
XM_005269009.3:c.4258del	XP_005269066.1:p.Thr1420ArgfsTer20
XM_005269010.3:c.4240del	XP_005269067.1:p.Thr1414ArgfsTer20
XM_005269011.3:c.4225del	XP_005269068.1:p.Thr1409ArgfsTer20
XM_005269012.3:c.4150del	XP_005269069.1:p.Thr1384ArgfsTer20
XM_005269013.3:c.4135del	XP_005269070.1:p.Thr1379ArgfsTer20
XM_005269014.3:c.4096del	XP_005269071.1:p.Thr1366ArgfsTer20
XM_006719493.3:c.4219del	XP_006719556.1:p.Thr1407ArgfsTer20
XM_006719494.3:c.4147del	XP_006719557.1:p.Thr1383ArgfsTer20
XM_011538556.3:c.4210del	XP_011536858.1:p.Thr1404ArgfsTer20
XM_017019607.2:c.4225del	XP_016875096.1:p.Thr1409ArgfsTer20
XM_017019608.2:c.4186del	XP_016875097.1:p.Thr1396ArgfsTer20
XM_017019609.2:c.4075del	XP_016875098.1:p.Thr1359ArgfsTer20
XM_017019610.2:c.4075del	XP_016875099.1:p.Thr1359ArgfsTer20
XM_017019611.2:c.4057del	XP_016875100.1:p.Thr1353ArgfsTer20
NM_001173463.2:c.4165del	NP_001166934.1:p.Thr1389ArgfsTer20
NM_001173464.2:c.4276del MANE Select	NP_001166935.1:p.Thr1426ArgfsTer20
NM_001173465.2:c.4117del	NP_001166936.1:p.Thr1373ArgfsTer20
NM_017641.4:c.4237del	NP_060111.2:p.Thr1413ArgfsTer20
NM_001378439.1:c.4279del	NP_001365368.1:p.Thr1427ArgfsTer20
NM_001378440.1:c.4264del	NP_001365369.1:p.Thr1422ArgfsTer20
NM_001378441.1:c.4240del	NP_001365370.1:p.Thr1414ArgfsTer20