Canonical Allele Identifier: CA384386899

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703418C>G (hg19) ; chr12:g.39309616C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309616C>G , CM000674.2:g.39309616C>G	GRCh38
NC_000012.11:g.39703418C>G , CM000674.1:g.39703418C>G	GRCh37
NC_000012.10:g.37989685C>G	NCBI36
NG_017067.1:g.138775G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4247G>C MANE Select	ENSP00000354878.5:p.Arg1416Thr
ENST00000636569.1:c.4184G>C	ENSP00000490369.1:p.Arg1395Thr
ENST00000361418.9:c.4247G>C	ENSP00000354878.5:p.Arg1416Thr
ENST00000361961.7:c.4208G>C	ENSP00000354851.3:p.Arg1403Thr
ENST00000541463.6:c.4088G>C	ENSP00000438075.2:p.Arg1363Thr
ENST00000544797.6:c.4136G>C	ENSP00000445606.2:p.Arg1379Thr
ENST00000547733.1:n.1561G>C
ENST00000551264.5:c.1190G>C	ENSP00000448792.1:p.Arg397Thr
ENST00000552961.5:c.2149G>C
NM_001173463.1:c.4136G>C	NP_001166934.1:p.Arg1379Thr
NM_001173464.1:c.4247G>C	NP_001166935.1:p.Arg1416Thr
NM_001173465.1:c.4088G>C	NP_001166936.1:p.Arg1363Thr
NM_017641.3:c.4208G>C	NP_060111.2:p.Arg1403Thr
XM_005269007.1:c.4250G>C	XP_005269064.1:p.Arg1417Thr
XM_005269008.1:c.4235G>C	XP_005269065.1:p.Arg1412Thr
XM_005269009.1:c.4229G>C	XP_005269066.1:p.Arg1410Thr
XM_005269010.1:c.4211G>C	XP_005269067.1:p.Arg1404Thr
XM_005269011.1:c.4196G>C	XP_005269068.1:p.Arg1399Thr
XM_005269012.1:c.4121G>C	XP_005269069.1:p.Arg1374Thr
XM_005269013.1:c.4106G>C	XP_005269070.1:p.Arg1369Thr
XM_005269014.1:c.4067G>C	XP_005269071.1:p.Arg1356Thr
XM_006719493.1:c.4190G>C	XP_006719556.1:p.Arg1397Thr
XM_006719494.1:c.4118G>C	XP_006719557.1:p.Arg1373Thr
XM_006719496.1:c.4175G>C	XP_006719559.1:p.Arg1392Thr
XM_011538556.1:c.4181G>C	XP_011536858.1:p.Arg1394Thr
XM_005269007.3:c.4250G>C	XP_005269064.1:p.Arg1417Thr
XM_005269008.3:c.4235G>C	XP_005269065.1:p.Arg1412Thr
XM_005269009.3:c.4229G>C	XP_005269066.1:p.Arg1410Thr
XM_005269010.3:c.4211G>C	XP_005269067.1:p.Arg1404Thr
XM_005269011.3:c.4196G>C	XP_005269068.1:p.Arg1399Thr
XM_005269012.3:c.4121G>C	XP_005269069.1:p.Arg1374Thr
XM_005269013.3:c.4106G>C	XP_005269070.1:p.Arg1369Thr
XM_005269014.3:c.4067G>C	XP_005269071.1:p.Arg1356Thr
XM_006719493.3:c.4190G>C	XP_006719556.1:p.Arg1397Thr
XM_006719494.3:c.4118G>C	XP_006719557.1:p.Arg1373Thr
XM_011538556.3:c.4181G>C	XP_011536858.1:p.Arg1394Thr
XM_017019607.2:c.4196G>C	XP_016875096.1:p.Arg1399Thr
XM_017019608.2:c.4157G>C	XP_016875097.1:p.Arg1386Thr
XM_017019609.2:c.4046G>C	XP_016875098.1:p.Arg1349Thr
XM_017019610.2:c.4046G>C	XP_016875099.1:p.Arg1349Thr
XM_017019611.2:c.4028G>C	XP_016875100.1:p.Arg1343Thr
NM_001173463.2:c.4136G>C	NP_001166934.1:p.Arg1379Thr
NM_001173464.2:c.4247G>C MANE Select	NP_001166935.1:p.Arg1416Thr
NM_001173465.2:c.4088G>C	NP_001166936.1:p.Arg1363Thr
NM_017641.4:c.4208G>C	NP_060111.2:p.Arg1403Thr
NM_001378439.1:c.4250G>C	NP_001365368.1:p.Arg1417Thr
NM_001378440.1:c.4235G>C	NP_001365369.1:p.Arg1412Thr
NM_001378441.1:c.4211G>C	NP_001365370.1:p.Arg1404Thr