Canonical Allele Identifier: CA384386767

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703395T>A (hg19) ; chr12:g.39309593T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309593T>A , CM000674.2:g.39309593T>A	GRCh38
NC_000012.11:g.39703395T>A , CM000674.1:g.39703395T>A	GRCh37
NC_000012.10:g.37989662T>A	NCBI36
NG_017067.1:g.138798A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4270A>T MANE Select	ENSP00000354878.5:p.Thr1424Ser
ENST00000636569.1:c.4207A>T	ENSP00000490369.1:p.Thr1403Ser
ENST00000361418.9:c.4270A>T	ENSP00000354878.5:p.Thr1424Ser
ENST00000361961.7:c.4231A>T	ENSP00000354851.3:p.Thr1411Ser
ENST00000541463.6:c.4111A>T	ENSP00000438075.2:p.Thr1371Ser
ENST00000544797.6:c.4159A>T	ENSP00000445606.2:p.Thr1387Ser
ENST00000547733.1:n.1584A>T
ENST00000551264.5:c.1213A>T	ENSP00000448792.1:p.Thr405Ser
ENST00000552961.5:c.2172A>T
NM_001173463.1:c.4159A>T	NP_001166934.1:p.Thr1387Ser
NM_001173464.1:c.4270A>T	NP_001166935.1:p.Thr1424Ser
NM_001173465.1:c.4111A>T	NP_001166936.1:p.Thr1371Ser
NM_017641.3:c.4231A>T	NP_060111.2:p.Thr1411Ser
XM_005269007.1:c.4273A>T	XP_005269064.1:p.Thr1425Ser
XM_005269008.1:c.4258A>T	XP_005269065.1:p.Thr1420Ser
XM_005269009.1:c.4252A>T	XP_005269066.1:p.Thr1418Ser
XM_005269010.1:c.4234A>T	XP_005269067.1:p.Thr1412Ser
XM_005269011.1:c.4219A>T	XP_005269068.1:p.Thr1407Ser
XM_005269012.1:c.4144A>T	XP_005269069.1:p.Thr1382Ser
XM_005269013.1:c.4129A>T	XP_005269070.1:p.Thr1377Ser
XM_005269014.1:c.4090A>T	XP_005269071.1:p.Thr1364Ser
XM_006719493.1:c.4213A>T	XP_006719556.1:p.Thr1405Ser
XM_006719494.1:c.4141A>T	XP_006719557.1:p.Thr1381Ser
XM_006719496.1:c.4198A>T	XP_006719559.1:p.Thr1400Ser
XM_011538556.1:c.4204A>T	XP_011536858.1:p.Thr1402Ser
XM_005269007.3:c.4273A>T	XP_005269064.1:p.Thr1425Ser
XM_005269008.3:c.4258A>T	XP_005269065.1:p.Thr1420Ser
XM_005269009.3:c.4252A>T	XP_005269066.1:p.Thr1418Ser
XM_005269010.3:c.4234A>T	XP_005269067.1:p.Thr1412Ser
XM_005269011.3:c.4219A>T	XP_005269068.1:p.Thr1407Ser
XM_005269012.3:c.4144A>T	XP_005269069.1:p.Thr1382Ser
XM_005269013.3:c.4129A>T	XP_005269070.1:p.Thr1377Ser
XM_005269014.3:c.4090A>T	XP_005269071.1:p.Thr1364Ser
XM_006719493.3:c.4213A>T	XP_006719556.1:p.Thr1405Ser
XM_006719494.3:c.4141A>T	XP_006719557.1:p.Thr1381Ser
XM_011538556.3:c.4204A>T	XP_011536858.1:p.Thr1402Ser
XM_017019607.2:c.4219A>T	XP_016875096.1:p.Thr1407Ser
XM_017019608.2:c.4180A>T	XP_016875097.1:p.Thr1394Ser
XM_017019609.2:c.4069A>T	XP_016875098.1:p.Thr1357Ser
XM_017019610.2:c.4069A>T	XP_016875099.1:p.Thr1357Ser
XM_017019611.2:c.4051A>T	XP_016875100.1:p.Thr1351Ser
NM_001173463.2:c.4159A>T	NP_001166934.1:p.Thr1387Ser
NM_001173464.2:c.4270A>T MANE Select	NP_001166935.1:p.Thr1424Ser
NM_001173465.2:c.4111A>T	NP_001166936.1:p.Thr1371Ser
NM_017641.4:c.4231A>T	NP_060111.2:p.Thr1411Ser
NM_001378439.1:c.4273A>T	NP_001365368.1:p.Thr1425Ser
NM_001378440.1:c.4258A>T	NP_001365369.1:p.Thr1420Ser
NM_001378441.1:c.4234A>T	NP_001365370.1:p.Thr1412Ser