Canonical Allele Identifier: CA384387124

Gene: KIF21A

Linked Data

• gnomAD v4: 12-39309652-G-A
• MyVariant Identifiers: chr12:g.39703454G>A (hg19) ; chr12:g.39309652G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309652G>A , CM000674.2:g.39309652G>A	GRCh38
NC_000012.11:g.39703454G>A , CM000674.1:g.39703454G>A	GRCh37
NC_000012.10:g.37989721G>A	NCBI36
NG_017067.1:g.138739C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4211C>T MANE Select	ENSP00000354878.5:p.Thr1404Ile
ENST00000636569.1:c.4148C>T	ENSP00000490369.1:p.Thr1383Ile
ENST00000361418.9:c.4211C>T	ENSP00000354878.5:p.Thr1404Ile
ENST00000361961.7:c.4172C>T	ENSP00000354851.3:p.Thr1391Ile
ENST00000541463.6:c.4052C>T	ENSP00000438075.2:p.Thr1351Ile
ENST00000544797.6:c.4100C>T	ENSP00000445606.2:p.Thr1367Ile
ENST00000547733.1:n.1525C>T
ENST00000551264.5:c.1154C>T	ENSP00000448792.1:p.Thr385Ile
ENST00000552961.5:c.2113C>T
NM_001173463.1:c.4100C>T	NP_001166934.1:p.Thr1367Ile
NM_001173464.1:c.4211C>T	NP_001166935.1:p.Thr1404Ile
NM_001173465.1:c.4052C>T	NP_001166936.1:p.Thr1351Ile
NM_017641.3:c.4172C>T	NP_060111.2:p.Thr1391Ile
XM_005269007.1:c.4214C>T	XP_005269064.1:p.Thr1405Ile
XM_005269008.1:c.4199C>T	XP_005269065.1:p.Thr1400Ile
XM_005269009.1:c.4193C>T	XP_005269066.1:p.Thr1398Ile
XM_005269010.1:c.4175C>T	XP_005269067.1:p.Thr1392Ile
XM_005269011.1:c.4160C>T	XP_005269068.1:p.Thr1387Ile
XM_005269012.1:c.4085C>T	XP_005269069.1:p.Thr1362Ile
XM_005269013.1:c.4070C>T	XP_005269070.1:p.Thr1357Ile
XM_005269014.1:c.4031C>T	XP_005269071.1:p.Thr1344Ile
XM_006719493.1:c.4154C>T	XP_006719556.1:p.Thr1385Ile
XM_006719494.1:c.4082C>T	XP_006719557.1:p.Thr1361Ile
XM_006719496.1:c.4139C>T	XP_006719559.1:p.Thr1380Ile
XM_011538556.1:c.4145C>T	XP_011536858.1:p.Thr1382Ile
XM_005269007.3:c.4214C>T	XP_005269064.1:p.Thr1405Ile
XM_005269008.3:c.4199C>T	XP_005269065.1:p.Thr1400Ile
XM_005269009.3:c.4193C>T	XP_005269066.1:p.Thr1398Ile
XM_005269010.3:c.4175C>T	XP_005269067.1:p.Thr1392Ile
XM_005269011.3:c.4160C>T	XP_005269068.1:p.Thr1387Ile
XM_005269012.3:c.4085C>T	XP_005269069.1:p.Thr1362Ile
XM_005269013.3:c.4070C>T	XP_005269070.1:p.Thr1357Ile
XM_005269014.3:c.4031C>T	XP_005269071.1:p.Thr1344Ile
XM_006719493.3:c.4154C>T	XP_006719556.1:p.Thr1385Ile
XM_006719494.3:c.4082C>T	XP_006719557.1:p.Thr1361Ile
XM_011538556.3:c.4145C>T	XP_011536858.1:p.Thr1382Ile
XM_017019607.2:c.4160C>T	XP_016875096.1:p.Thr1387Ile
XM_017019608.2:c.4121C>T	XP_016875097.1:p.Thr1374Ile
XM_017019609.2:c.4010C>T	XP_016875098.1:p.Thr1337Ile
XM_017019610.2:c.4010C>T	XP_016875099.1:p.Thr1337Ile
XM_017019611.2:c.3992C>T	XP_016875100.1:p.Thr1331Ile
NM_001173463.2:c.4100C>T	NP_001166934.1:p.Thr1367Ile
NM_001173464.2:c.4211C>T MANE Select	NP_001166935.1:p.Thr1404Ile
NM_001173465.2:c.4052C>T	NP_001166936.1:p.Thr1351Ile
NM_017641.4:c.4172C>T	NP_060111.2:p.Thr1391Ile
NM_001378439.1:c.4214C>T	NP_001365368.1:p.Thr1405Ile
NM_001378440.1:c.4199C>T	NP_001365369.1:p.Thr1400Ile
NM_001378441.1:c.4175C>T	NP_001365370.1:p.Thr1392Ile