Canonical Allele Identifier: CA384386740

Gene: KIF21A

Linked Data

• gnomAD v4: 12-39309586-G-T
• MyVariant Identifiers: chr12:g.39703388G>T (hg19) ; chr12:g.39309586G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000361418.10:c.4277C>A MANE Select	ENSP00000354878.5:p.Thr1426Lys
ENST00000636569.1:c.4214C>A	ENSP00000490369.1:p.Thr1405Lys
ENST00000361418.9:c.4277C>A	ENSP00000354878.5:p.Thr1426Lys
ENST00000361961.7:c.4238C>A	ENSP00000354851.3:p.Thr1413Lys
ENST00000541463.6:c.4118C>A	ENSP00000438075.2:p.Thr1373Lys
ENST00000544797.6:c.4166C>A	ENSP00000445606.2:p.Thr1389Lys
ENST00000547733.1:n.1591C>A
ENST00000551264.5:c.1220C>A	ENSP00000448792.1:p.Thr407Lys
ENST00000552961.5:c.2179C>A
NM_001173463.1:c.4166C>A	NP_001166934.1:p.Thr1389Lys
NM_001173464.1:c.4277C>A	NP_001166935.1:p.Thr1426Lys
NM_001173465.1:c.4118C>A	NP_001166936.1:p.Thr1373Lys
NM_017641.3:c.4238C>A	NP_060111.2:p.Thr1413Lys
XM_005269007.1:c.4280C>A	XP_005269064.1:p.Thr1427Lys
XM_005269008.1:c.4265C>A	XP_005269065.1:p.Thr1422Lys
XM_005269009.1:c.4259C>A	XP_005269066.1:p.Thr1420Lys
XM_005269010.1:c.4241C>A	XP_005269067.1:p.Thr1414Lys
XM_005269011.1:c.4226C>A	XP_005269068.1:p.Thr1409Lys
XM_005269012.1:c.4151C>A	XP_005269069.1:p.Thr1384Lys
XM_005269013.1:c.4136C>A	XP_005269070.1:p.Thr1379Lys
XM_005269014.1:c.4097C>A	XP_005269071.1:p.Thr1366Lys
XM_006719493.1:c.4220C>A	XP_006719556.1:p.Thr1407Lys
XM_006719494.1:c.4148C>A	XP_006719557.1:p.Thr1383Lys
XM_006719496.1:c.4205C>A	XP_006719559.1:p.Thr1402Lys
XM_011538556.1:c.4211C>A	XP_011536858.1:p.Thr1404Lys
XM_005269007.3:c.4280C>A	XP_005269064.1:p.Thr1427Lys
XM_005269008.3:c.4265C>A	XP_005269065.1:p.Thr1422Lys
XM_005269009.3:c.4259C>A	XP_005269066.1:p.Thr1420Lys
XM_005269010.3:c.4241C>A	XP_005269067.1:p.Thr1414Lys
XM_005269011.3:c.4226C>A	XP_005269068.1:p.Thr1409Lys
XM_005269012.3:c.4151C>A	XP_005269069.1:p.Thr1384Lys
XM_005269013.3:c.4136C>A	XP_005269070.1:p.Thr1379Lys
XM_005269014.3:c.4097C>A	XP_005269071.1:p.Thr1366Lys
XM_006719493.3:c.4220C>A	XP_006719556.1:p.Thr1407Lys
XM_006719494.3:c.4148C>A	XP_006719557.1:p.Thr1383Lys
XM_011538556.3:c.4211C>A	XP_011536858.1:p.Thr1404Lys
XM_017019607.2:c.4226C>A	XP_016875096.1:p.Thr1409Lys
XM_017019608.2:c.4187C>A	XP_016875097.1:p.Thr1396Lys
XM_017019609.2:c.4076C>A	XP_016875098.1:p.Thr1359Lys
XM_017019610.2:c.4076C>A	XP_016875099.1:p.Thr1359Lys
XM_017019611.2:c.4058C>A	XP_016875100.1:p.Thr1353Lys
NM_001173463.2:c.4166C>A	NP_001166934.1:p.Thr1389Lys
NM_001173464.2:c.4277C>A MANE Select	NP_001166935.1:p.Thr1426Lys
NM_001173465.2:c.4118C>A	NP_001166936.1:p.Thr1373Lys
NM_017641.4:c.4238C>A	NP_060111.2:p.Thr1413Lys
NM_001378439.1:c.4280C>A	NP_001365368.1:p.Thr1427Lys
NM_001378440.1:c.4265C>A	NP_001365369.1:p.Thr1422Lys
NM_001378441.1:c.4241C>A	NP_001365370.1:p.Thr1414Lys