Canonical Allele Identifier: CA384387110

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703449A>C (hg19) ; chr12:g.39309647A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309647A>C , CM000674.2:g.39309647A>C	GRCh38
NC_000012.11:g.39703449A>C , CM000674.1:g.39703449A>C	GRCh37
NC_000012.10:g.37989716A>C	NCBI36
NG_017067.1:g.138744T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4216T>G MANE Select	ENSP00000354878.5:p.Ser1406Ala
ENST00000636569.1:c.4153T>G	ENSP00000490369.1:p.Ser1385Ala
ENST00000361418.9:c.4216T>G	ENSP00000354878.5:p.Ser1406Ala
ENST00000361961.7:c.4177T>G	ENSP00000354851.3:p.Ser1393Ala
ENST00000541463.6:c.4057T>G	ENSP00000438075.2:p.Ser1353Ala
ENST00000544797.6:c.4105T>G	ENSP00000445606.2:p.Ser1369Ala
ENST00000547733.1:n.1530T>G
ENST00000551264.5:c.1159T>G	ENSP00000448792.1:p.Ser387Ala
ENST00000552961.5:c.2118T>G
NM_001173463.1:c.4105T>G	NP_001166934.1:p.Ser1369Ala
NM_001173464.1:c.4216T>G	NP_001166935.1:p.Ser1406Ala
NM_001173465.1:c.4057T>G	NP_001166936.1:p.Ser1353Ala
NM_017641.3:c.4177T>G	NP_060111.2:p.Ser1393Ala
XM_005269007.1:c.4219T>G	XP_005269064.1:p.Ser1407Ala
XM_005269008.1:c.4204T>G	XP_005269065.1:p.Ser1402Ala
XM_005269009.1:c.4198T>G	XP_005269066.1:p.Ser1400Ala
XM_005269010.1:c.4180T>G	XP_005269067.1:p.Ser1394Ala
XM_005269011.1:c.4165T>G	XP_005269068.1:p.Ser1389Ala
XM_005269012.1:c.4090T>G	XP_005269069.1:p.Ser1364Ala
XM_005269013.1:c.4075T>G	XP_005269070.1:p.Ser1359Ala
XM_005269014.1:c.4036T>G	XP_005269071.1:p.Ser1346Ala
XM_006719493.1:c.4159T>G	XP_006719556.1:p.Ser1387Ala
XM_006719494.1:c.4087T>G	XP_006719557.1:p.Ser1363Ala
XM_006719496.1:c.4144T>G	XP_006719559.1:p.Ser1382Ala
XM_011538556.1:c.4150T>G	XP_011536858.1:p.Ser1384Ala
XM_005269007.3:c.4219T>G	XP_005269064.1:p.Ser1407Ala
XM_005269008.3:c.4204T>G	XP_005269065.1:p.Ser1402Ala
XM_005269009.3:c.4198T>G	XP_005269066.1:p.Ser1400Ala
XM_005269010.3:c.4180T>G	XP_005269067.1:p.Ser1394Ala
XM_005269011.3:c.4165T>G	XP_005269068.1:p.Ser1389Ala
XM_005269012.3:c.4090T>G	XP_005269069.1:p.Ser1364Ala
XM_005269013.3:c.4075T>G	XP_005269070.1:p.Ser1359Ala
XM_005269014.3:c.4036T>G	XP_005269071.1:p.Ser1346Ala
XM_006719493.3:c.4159T>G	XP_006719556.1:p.Ser1387Ala
XM_006719494.3:c.4087T>G	XP_006719557.1:p.Ser1363Ala
XM_011538556.3:c.4150T>G	XP_011536858.1:p.Ser1384Ala
XM_017019607.2:c.4165T>G	XP_016875096.1:p.Ser1389Ala
XM_017019608.2:c.4126T>G	XP_016875097.1:p.Ser1376Ala
XM_017019609.2:c.4015T>G	XP_016875098.1:p.Ser1339Ala
XM_017019610.2:c.4015T>G	XP_016875099.1:p.Ser1339Ala
XM_017019611.2:c.3997T>G	XP_016875100.1:p.Ser1333Ala
NM_001173463.2:c.4105T>G	NP_001166934.1:p.Ser1369Ala
NM_001173464.2:c.4216T>G MANE Select	NP_001166935.1:p.Ser1406Ala
NM_001173465.2:c.4057T>G	NP_001166936.1:p.Ser1353Ala
NM_017641.4:c.4177T>G	NP_060111.2:p.Ser1393Ala
NM_001378439.1:c.4219T>G	NP_001365368.1:p.Ser1407Ala
NM_001378440.1:c.4204T>G	NP_001365369.1:p.Ser1402Ala
NM_001378441.1:c.4180T>G	NP_001365370.1:p.Ser1394Ala