Canonical Allele Identifier: CA384386742

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703388G>C (hg19) ; chr12:g.39309586G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309586G>C , CM000674.2:g.39309586G>C	GRCh38
NC_000012.11:g.39703388G>C , CM000674.1:g.39703388G>C	GRCh37
NC_000012.10:g.37989655G>C	NCBI36
NG_017067.1:g.138805C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000361418.10:c.4277C>G MANE Select	ENSP00000354878.5:p.Thr1426Arg
ENST00000636569.1:c.4214C>G	ENSP00000490369.1:p.Thr1405Arg
ENST00000361418.9:c.4277C>G	ENSP00000354878.5:p.Thr1426Arg
ENST00000361961.7:c.4238C>G	ENSP00000354851.3:p.Thr1413Arg
ENST00000541463.6:c.4118C>G	ENSP00000438075.2:p.Thr1373Arg
ENST00000544797.6:c.4166C>G	ENSP00000445606.2:p.Thr1389Arg
ENST00000547733.1:n.1591C>G
ENST00000551264.5:c.1220C>G	ENSP00000448792.1:p.Thr407Arg
ENST00000552961.5:c.2179C>G
NM_001173463.1:c.4166C>G	NP_001166934.1:p.Thr1389Arg
NM_001173464.1:c.4277C>G	NP_001166935.1:p.Thr1426Arg
NM_001173465.1:c.4118C>G	NP_001166936.1:p.Thr1373Arg
NM_017641.3:c.4238C>G	NP_060111.2:p.Thr1413Arg
XM_005269007.1:c.4280C>G	XP_005269064.1:p.Thr1427Arg
XM_005269008.1:c.4265C>G	XP_005269065.1:p.Thr1422Arg
XM_005269009.1:c.4259C>G	XP_005269066.1:p.Thr1420Arg
XM_005269010.1:c.4241C>G	XP_005269067.1:p.Thr1414Arg
XM_005269011.1:c.4226C>G	XP_005269068.1:p.Thr1409Arg
XM_005269012.1:c.4151C>G	XP_005269069.1:p.Thr1384Arg
XM_005269013.1:c.4136C>G	XP_005269070.1:p.Thr1379Arg
XM_005269014.1:c.4097C>G	XP_005269071.1:p.Thr1366Arg
XM_006719493.1:c.4220C>G	XP_006719556.1:p.Thr1407Arg
XM_006719494.1:c.4148C>G	XP_006719557.1:p.Thr1383Arg
XM_006719496.1:c.4205C>G	XP_006719559.1:p.Thr1402Arg
XM_011538556.1:c.4211C>G	XP_011536858.1:p.Thr1404Arg
XM_005269007.3:c.4280C>G	XP_005269064.1:p.Thr1427Arg
XM_005269008.3:c.4265C>G	XP_005269065.1:p.Thr1422Arg
XM_005269009.3:c.4259C>G	XP_005269066.1:p.Thr1420Arg
XM_005269010.3:c.4241C>G	XP_005269067.1:p.Thr1414Arg
XM_005269011.3:c.4226C>G	XP_005269068.1:p.Thr1409Arg
XM_005269012.3:c.4151C>G	XP_005269069.1:p.Thr1384Arg
XM_005269013.3:c.4136C>G	XP_005269070.1:p.Thr1379Arg
XM_005269014.3:c.4097C>G	XP_005269071.1:p.Thr1366Arg
XM_006719493.3:c.4220C>G	XP_006719556.1:p.Thr1407Arg
XM_006719494.3:c.4148C>G	XP_006719557.1:p.Thr1383Arg
XM_011538556.3:c.4211C>G	XP_011536858.1:p.Thr1404Arg
XM_017019607.2:c.4226C>G	XP_016875096.1:p.Thr1409Arg
XM_017019608.2:c.4187C>G	XP_016875097.1:p.Thr1396Arg
XM_017019609.2:c.4076C>G	XP_016875098.1:p.Thr1359Arg
XM_017019610.2:c.4076C>G	XP_016875099.1:p.Thr1359Arg
XM_017019611.2:c.4058C>G	XP_016875100.1:p.Thr1353Arg
NM_001173463.2:c.4166C>G	NP_001166934.1:p.Thr1389Arg
NM_001173464.2:c.4277C>G MANE Select	NP_001166935.1:p.Thr1426Arg
NM_001173465.2:c.4118C>G	NP_001166936.1:p.Thr1373Arg
NM_017641.4:c.4238C>G	NP_060111.2:p.Thr1413Arg
NM_001378439.1:c.4280C>G	NP_001365368.1:p.Thr1427Arg
NM_001378440.1:c.4265C>G	NP_001365369.1:p.Thr1422Arg
NM_001378441.1:c.4241C>G	NP_001365370.1:p.Thr1414Arg