Canonical Allele Identifier: CA10641118

Gene: KIF21A

Linked Data

• ClinVar Variation Id: 308550
• ClinVar RCV Id: RCV000287324
• dbSNP Id: rs886049340
• MyVariant Identifiers: chr12:g.39698655T>G (hg19) ; chr12:g.39304853T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39304853T>G , CM000674.2:g.39304853T>G	GRCh38
NC_000012.11:g.39698655T>G , CM000674.1:g.39698655T>G	GRCh37
NC_000012.10:g.37984922T>G	NCBI36
NG_017067.1:g.143538A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4528A>C MANE Select	ENSP00000354878.5:p.Ile1510Leu
ENST00000636569.1:c.4465A>C	ENSP00000490369.1:p.Ile1489Leu
ENST00000361418.9:c.4528A>C	ENSP00000354878.5:p.Ile1510Leu
ENST00000361961.7:c.4489A>C	ENSP00000354851.3:p.Ile1497Leu
ENST00000541463.6:c.4369A>C	ENSP00000438075.2:p.Ile1457Leu
ENST00000544797.6:c.4417A>C	ENSP00000445606.2:p.Ile1473Leu
ENST00000547733.1:n.1842A>C
ENST00000551264.5:c.1471A>C	ENSP00000448792.1:p.Ile491Leu
ENST00000552961.5:c.2430A>C
NM_001173463.1:c.4417A>C	NP_001166934.1:p.Ile1473Leu
NM_001173464.1:c.4528A>C	NP_001166935.1:p.Ile1510Leu
NM_001173465.1:c.4369A>C	NP_001166936.1:p.Ile1457Leu
NM_017641.3:c.4489A>C	NP_060111.2:p.Ile1497Leu
XM_005269007.1:c.4531A>C	XP_005269064.1:p.Ile1511Leu
XM_005269008.1:c.4516A>C	XP_005269065.1:p.Ile1506Leu
XM_005269009.1:c.4510A>C	XP_005269066.1:p.Ile1504Leu
XM_005269010.1:c.4492A>C	XP_005269067.1:p.Ile1498Leu
XM_005269011.1:c.4477A>C	XP_005269068.1:p.Ile1493Leu
XM_005269012.1:c.4402A>C	XP_005269069.1:p.Ile1468Leu
XM_005269013.1:c.4387A>C	XP_005269070.1:p.Ile1463Leu
XM_005269014.1:c.4348A>C	XP_005269071.1:p.Ile1450Leu
XM_006719493.1:c.4471A>C	XP_006719556.1:p.Ile1491Leu
XM_006719494.1:c.4399A>C	XP_006719557.1:p.Ile1467Leu
XM_006719496.1:c.4456A>C	XP_006719559.1:p.Ile1486Leu
XM_011538556.1:c.4462A>C	XP_011536858.1:p.Ile1488Leu
XM_005269007.3:c.4531A>C	XP_005269064.1:p.Ile1511Leu
XM_005269008.3:c.4516A>C	XP_005269065.1:p.Ile1506Leu
XM_005269009.3:c.4510A>C	XP_005269066.1:p.Ile1504Leu
XM_005269010.3:c.4492A>C	XP_005269067.1:p.Ile1498Leu
XM_005269011.3:c.4477A>C	XP_005269068.1:p.Ile1493Leu
XM_005269012.3:c.4402A>C	XP_005269069.1:p.Ile1468Leu
XM_005269013.3:c.4387A>C	XP_005269070.1:p.Ile1463Leu
XM_005269014.3:c.4348A>C	XP_005269071.1:p.Ile1450Leu
XM_006719493.3:c.4471A>C	XP_006719556.1:p.Ile1491Leu
XM_006719494.3:c.4399A>C	XP_006719557.1:p.Ile1467Leu
XM_011538556.3:c.4462A>C	XP_011536858.1:p.Ile1488Leu
XM_017019607.2:c.4477A>C	XP_016875096.1:p.Ile1493Leu
XM_017019608.2:c.4438A>C	XP_016875097.1:p.Ile1480Leu
XM_017019609.2:c.4327A>C	XP_016875098.1:p.Ile1443Leu
XM_017019610.2:c.4327A>C	XP_016875099.1:p.Ile1443Leu
XM_017019611.2:c.4309A>C	XP_016875100.1:p.Ile1437Leu
NM_001173463.2:c.4417A>C	NP_001166934.1:p.Ile1473Leu
NM_001173464.2:c.4528A>C MANE Select	NP_001166935.1:p.Ile1510Leu
NM_001173465.2:c.4369A>C	NP_001166936.1:p.Ile1457Leu
NM_017641.4:c.4489A>C	NP_060111.2:p.Ile1497Leu
NM_001378439.1:c.4531A>C	NP_001365368.1:p.Ile1511Leu
NM_001378440.1:c.4516A>C	NP_001365369.1:p.Ile1506Leu
NM_001378441.1:c.4492A>C	NP_001365370.1:p.Ile1498Leu