Canonical Allele Identifier: CA10642067

Gene: KIF21A

Linked Data

• ClinVar Variation Id: 308553
• ClinVar RCV Id: RCV000281544
• dbSNP Id: rs886049341
• gnomAD v4: 12-39309599-T-C
• MyVariant Identifiers: chr12:g.39703401T>C (hg19) ; chr12:g.39309599T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309599T>C , CM000674.2:g.39309599T>C	GRCh38
NC_000012.11:g.39703401T>C , CM000674.1:g.39703401T>C	GRCh37
NC_000012.10:g.37989668T>C	NCBI36
NG_017067.1:g.138792A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000361418.10:c.4264A>G MANE Select	ENSP00000354878.5:p.Ile1422Val
ENST00000636569.1:c.4201A>G	ENSP00000490369.1:p.Ile1401Val
ENST00000361418.9:c.4264A>G	ENSP00000354878.5:p.Ile1422Val
ENST00000361961.7:c.4225A>G	ENSP00000354851.3:p.Ile1409Val
ENST00000541463.6:c.4105A>G	ENSP00000438075.2:p.Ile1369Val
ENST00000544797.6:c.4153A>G	ENSP00000445606.2:p.Ile1385Val
ENST00000547733.1:n.1578A>G
ENST00000551264.5:c.1207A>G	ENSP00000448792.1:p.Ile403Val
ENST00000552961.5:c.2166A>G
NM_001173463.1:c.4153A>G	NP_001166934.1:p.Ile1385Val
NM_001173464.1:c.4264A>G	NP_001166935.1:p.Ile1422Val
NM_001173465.1:c.4105A>G	NP_001166936.1:p.Ile1369Val
NM_017641.3:c.4225A>G	NP_060111.2:p.Ile1409Val
XM_005269007.1:c.4267A>G	XP_005269064.1:p.Ile1423Val
XM_005269008.1:c.4252A>G	XP_005269065.1:p.Ile1418Val
XM_005269009.1:c.4246A>G	XP_005269066.1:p.Ile1416Val
XM_005269010.1:c.4228A>G	XP_005269067.1:p.Ile1410Val
XM_005269011.1:c.4213A>G	XP_005269068.1:p.Ile1405Val
XM_005269012.1:c.4138A>G	XP_005269069.1:p.Ile1380Val
XM_005269013.1:c.4123A>G	XP_005269070.1:p.Ile1375Val
XM_005269014.1:c.4084A>G	XP_005269071.1:p.Ile1362Val
XM_006719493.1:c.4207A>G	XP_006719556.1:p.Ile1403Val
XM_006719494.1:c.4135A>G	XP_006719557.1:p.Ile1379Val
XM_006719496.1:c.4192A>G	XP_006719559.1:p.Ile1398Val
XM_011538556.1:c.4198A>G	XP_011536858.1:p.Ile1400Val
XM_005269007.3:c.4267A>G	XP_005269064.1:p.Ile1423Val
XM_005269008.3:c.4252A>G	XP_005269065.1:p.Ile1418Val
XM_005269009.3:c.4246A>G	XP_005269066.1:p.Ile1416Val
XM_005269010.3:c.4228A>G	XP_005269067.1:p.Ile1410Val
XM_005269011.3:c.4213A>G	XP_005269068.1:p.Ile1405Val
XM_005269012.3:c.4138A>G	XP_005269069.1:p.Ile1380Val
XM_005269013.3:c.4123A>G	XP_005269070.1:p.Ile1375Val
XM_005269014.3:c.4084A>G	XP_005269071.1:p.Ile1362Val
XM_006719493.3:c.4207A>G	XP_006719556.1:p.Ile1403Val
XM_006719494.3:c.4135A>G	XP_006719557.1:p.Ile1379Val
XM_011538556.3:c.4198A>G	XP_011536858.1:p.Ile1400Val
XM_017019607.2:c.4213A>G	XP_016875096.1:p.Ile1405Val
XM_017019608.2:c.4174A>G	XP_016875097.1:p.Ile1392Val
XM_017019609.2:c.4063A>G	XP_016875098.1:p.Ile1355Val
XM_017019610.2:c.4063A>G	XP_016875099.1:p.Ile1355Val
XM_017019611.2:c.4045A>G	XP_016875100.1:p.Ile1349Val
NM_001173463.2:c.4153A>G	NP_001166934.1:p.Ile1385Val
NM_001173464.2:c.4264A>G MANE Select	NP_001166935.1:p.Ile1422Val
NM_001173465.2:c.4105A>G	NP_001166936.1:p.Ile1369Val
NM_017641.4:c.4225A>G	NP_060111.2:p.Ile1409Val
NM_001378439.1:c.4267A>G	NP_001365368.1:p.Ile1423Val
NM_001378440.1:c.4252A>G	NP_001365369.1:p.Ile1418Val
NM_001378441.1:c.4228A>G	NP_001365370.1:p.Ile1410Val