Canonical Allele Identifier: CA384386795

Gene: KIF21A

Linked Data

• gnomAD v4: 12-39309599-T-G
• MyVariant Identifiers: chr12:g.39703401T>G (hg19) ; chr12:g.39309599T>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000361418.10:c.4264A>C MANE Select	ENSP00000354878.5:p.Ile1422Leu
ENST00000636569.1:c.4201A>C	ENSP00000490369.1:p.Ile1401Leu
ENST00000361418.9:c.4264A>C	ENSP00000354878.5:p.Ile1422Leu
ENST00000361961.7:c.4225A>C	ENSP00000354851.3:p.Ile1409Leu
ENST00000541463.6:c.4105A>C	ENSP00000438075.2:p.Ile1369Leu
ENST00000544797.6:c.4153A>C	ENSP00000445606.2:p.Ile1385Leu
ENST00000547733.1:n.1578A>C
ENST00000551264.5:c.1207A>C	ENSP00000448792.1:p.Ile403Leu
ENST00000552961.5:c.2166A>C
NM_001173463.1:c.4153A>C	NP_001166934.1:p.Ile1385Leu
NM_001173464.1:c.4264A>C	NP_001166935.1:p.Ile1422Leu
NM_001173465.1:c.4105A>C	NP_001166936.1:p.Ile1369Leu
NM_017641.3:c.4225A>C	NP_060111.2:p.Ile1409Leu
XM_005269007.1:c.4267A>C	XP_005269064.1:p.Ile1423Leu
XM_005269008.1:c.4252A>C	XP_005269065.1:p.Ile1418Leu
XM_005269009.1:c.4246A>C	XP_005269066.1:p.Ile1416Leu
XM_005269010.1:c.4228A>C	XP_005269067.1:p.Ile1410Leu
XM_005269011.1:c.4213A>C	XP_005269068.1:p.Ile1405Leu
XM_005269012.1:c.4138A>C	XP_005269069.1:p.Ile1380Leu
XM_005269013.1:c.4123A>C	XP_005269070.1:p.Ile1375Leu
XM_005269014.1:c.4084A>C	XP_005269071.1:p.Ile1362Leu
XM_006719493.1:c.4207A>C	XP_006719556.1:p.Ile1403Leu
XM_006719494.1:c.4135A>C	XP_006719557.1:p.Ile1379Leu
XM_006719496.1:c.4192A>C	XP_006719559.1:p.Ile1398Leu
XM_011538556.1:c.4198A>C	XP_011536858.1:p.Ile1400Leu
XM_005269007.3:c.4267A>C	XP_005269064.1:p.Ile1423Leu
XM_005269008.3:c.4252A>C	XP_005269065.1:p.Ile1418Leu
XM_005269009.3:c.4246A>C	XP_005269066.1:p.Ile1416Leu
XM_005269010.3:c.4228A>C	XP_005269067.1:p.Ile1410Leu
XM_005269011.3:c.4213A>C	XP_005269068.1:p.Ile1405Leu
XM_005269012.3:c.4138A>C	XP_005269069.1:p.Ile1380Leu
XM_005269013.3:c.4123A>C	XP_005269070.1:p.Ile1375Leu
XM_005269014.3:c.4084A>C	XP_005269071.1:p.Ile1362Leu
XM_006719493.3:c.4207A>C	XP_006719556.1:p.Ile1403Leu
XM_006719494.3:c.4135A>C	XP_006719557.1:p.Ile1379Leu
XM_011538556.3:c.4198A>C	XP_011536858.1:p.Ile1400Leu
XM_017019607.2:c.4213A>C	XP_016875096.1:p.Ile1405Leu
XM_017019608.2:c.4174A>C	XP_016875097.1:p.Ile1392Leu
XM_017019609.2:c.4063A>C	XP_016875098.1:p.Ile1355Leu
XM_017019610.2:c.4063A>C	XP_016875099.1:p.Ile1355Leu
XM_017019611.2:c.4045A>C	XP_016875100.1:p.Ile1349Leu
NM_001173463.2:c.4153A>C	NP_001166934.1:p.Ile1385Leu
NM_001173464.2:c.4264A>C MANE Select	NP_001166935.1:p.Ile1422Leu
NM_001173465.2:c.4105A>C	NP_001166936.1:p.Ile1369Leu
NM_017641.4:c.4225A>C	NP_060111.2:p.Ile1409Leu
NM_001378439.1:c.4267A>C	NP_001365368.1:p.Ile1423Leu
NM_001378440.1:c.4252A>C	NP_001365369.1:p.Ile1418Leu
NM_001378441.1:c.4228A>C	NP_001365370.1:p.Ile1410Leu