Canonical Allele Identifier: CA384386745

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703389T>A (hg19) ; chr12:g.39309587T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309587T>A , CM000674.2:g.39309587T>A	GRCh38
NC_000012.11:g.39703389T>A , CM000674.1:g.39703389T>A	GRCh37
NC_000012.10:g.37989656T>A	NCBI36
NG_017067.1:g.138804A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000361418.10:c.4276A>T MANE Select	ENSP00000354878.5:p.Thr1426Ser
ENST00000636569.1:c.4213A>T	ENSP00000490369.1:p.Thr1405Ser
ENST00000361418.9:c.4276A>T	ENSP00000354878.5:p.Thr1426Ser
ENST00000361961.7:c.4237A>T	ENSP00000354851.3:p.Thr1413Ser
ENST00000541463.6:c.4117A>T	ENSP00000438075.2:p.Thr1373Ser
ENST00000544797.6:c.4165A>T	ENSP00000445606.2:p.Thr1389Ser
ENST00000547733.1:n.1590A>T
ENST00000551264.5:c.1219A>T	ENSP00000448792.1:p.Thr407Ser
ENST00000552961.5:c.2178A>T
NM_001173463.1:c.4165A>T	NP_001166934.1:p.Thr1389Ser
NM_001173464.1:c.4276A>T	NP_001166935.1:p.Thr1426Ser
NM_001173465.1:c.4117A>T	NP_001166936.1:p.Thr1373Ser
NM_017641.3:c.4237A>T	NP_060111.2:p.Thr1413Ser
XM_005269007.1:c.4279A>T	XP_005269064.1:p.Thr1427Ser
XM_005269008.1:c.4264A>T	XP_005269065.1:p.Thr1422Ser
XM_005269009.1:c.4258A>T	XP_005269066.1:p.Thr1420Ser
XM_005269010.1:c.4240A>T	XP_005269067.1:p.Thr1414Ser
XM_005269011.1:c.4225A>T	XP_005269068.1:p.Thr1409Ser
XM_005269012.1:c.4150A>T	XP_005269069.1:p.Thr1384Ser
XM_005269013.1:c.4135A>T	XP_005269070.1:p.Thr1379Ser
XM_005269014.1:c.4096A>T	XP_005269071.1:p.Thr1366Ser
XM_006719493.1:c.4219A>T	XP_006719556.1:p.Thr1407Ser
XM_006719494.1:c.4147A>T	XP_006719557.1:p.Thr1383Ser
XM_006719496.1:c.4204A>T	XP_006719559.1:p.Thr1402Ser
XM_011538556.1:c.4210A>T	XP_011536858.1:p.Thr1404Ser
XM_005269007.3:c.4279A>T	XP_005269064.1:p.Thr1427Ser
XM_005269008.3:c.4264A>T	XP_005269065.1:p.Thr1422Ser
XM_005269009.3:c.4258A>T	XP_005269066.1:p.Thr1420Ser
XM_005269010.3:c.4240A>T	XP_005269067.1:p.Thr1414Ser
XM_005269011.3:c.4225A>T	XP_005269068.1:p.Thr1409Ser
XM_005269012.3:c.4150A>T	XP_005269069.1:p.Thr1384Ser
XM_005269013.3:c.4135A>T	XP_005269070.1:p.Thr1379Ser
XM_005269014.3:c.4096A>T	XP_005269071.1:p.Thr1366Ser
XM_006719493.3:c.4219A>T	XP_006719556.1:p.Thr1407Ser
XM_006719494.3:c.4147A>T	XP_006719557.1:p.Thr1383Ser
XM_011538556.3:c.4210A>T	XP_011536858.1:p.Thr1404Ser
XM_017019607.2:c.4225A>T	XP_016875096.1:p.Thr1409Ser
XM_017019608.2:c.4186A>T	XP_016875097.1:p.Thr1396Ser
XM_017019609.2:c.4075A>T	XP_016875098.1:p.Thr1359Ser
XM_017019610.2:c.4075A>T	XP_016875099.1:p.Thr1359Ser
XM_017019611.2:c.4057A>T	XP_016875100.1:p.Thr1353Ser
NM_001173463.2:c.4165A>T	NP_001166934.1:p.Thr1389Ser
NM_001173464.2:c.4276A>T MANE Select	NP_001166935.1:p.Thr1426Ser
NM_001173465.2:c.4117A>T	NP_001166936.1:p.Thr1373Ser
NM_017641.4:c.4237A>T	NP_060111.2:p.Thr1413Ser
NM_001378439.1:c.4279A>T	NP_001365368.1:p.Thr1427Ser
NM_001378440.1:c.4264A>T	NP_001365369.1:p.Thr1422Ser
NM_001378441.1:c.4240A>T	NP_001365370.1:p.Thr1414Ser