Canonical Allele Identifier: CA384382757

Gene: KIF21A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39304868T>G , CM000674.2:g.39304868T>G	GRCh38
NC_000012.11:g.39698670T>G , CM000674.1:g.39698670T>G	GRCh37
NC_000012.10:g.37984937T>G	NCBI36
NG_017067.1:g.143523A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001173464.2:c.4513A>C MANE Select	NP_001166935.1:p.Ser1505Arg
ENST00000361418.10:c.4513A>C MANE Select	ENSP00000354878.5:p.Ser1505Arg
NM_001173463.1:c.4402A>C	NP_001166934.1:p.Ser1468Arg
NM_001173463.2:c.4402A>C	NP_001166934.1:p.Ser1468Arg
NM_001173464.1:c.4513A>C	NP_001166935.1:p.Ser1505Arg
NM_001173465.1:c.4354A>C	NP_001166936.1:p.Ser1452Arg
NM_001173465.2:c.4354A>C	NP_001166936.1:p.Ser1452Arg
NM_001378439.1:c.4516A>C	NP_001365368.1:p.Ser1506Arg
NM_001378440.1:c.4501A>C	NP_001365369.1:p.Ser1501Arg
NM_001378441.1:c.4477A>C	NP_001365370.1:p.Ser1493Arg
NM_017641.3:c.4474A>C	NP_060111.2:p.Ser1492Arg
NM_017641.4:c.4474A>C	NP_060111.2:p.Ser1492Arg
ENST00000361418.9:c.4513A>C	ENSP00000354878.5:p.Ser1505Arg
ENST00000361961.7:c.4474A>C	ENSP00000354851.3:p.Ser1492Arg
ENST00000541463.6:c.4354A>C	ENSP00000438075.2:p.Ser1452Arg
ENST00000544797.6:c.4402A>C	ENSP00000445606.2:p.Ser1468Arg
ENST00000547733.1:n.1827A>C
ENST00000551264.5:c.1456A>C	ENSP00000448792.1:p.Ser486Arg
ENST00000552961.5:c.2415A>C
ENST00000636569.1:c.4450A>C	ENSP00000490369.1:p.Ser1484Arg
XM_005269007.1:c.4516A>C	XP_005269064.1:p.Ser1506Arg
XM_005269007.3:c.4516A>C	XP_005269064.1:p.Ser1506Arg
XM_005269008.1:c.4501A>C	XP_005269065.1:p.Ser1501Arg
XM_005269008.3:c.4501A>C	XP_005269065.1:p.Ser1501Arg
XM_005269009.1:c.4495A>C	XP_005269066.1:p.Ser1499Arg
XM_005269009.3:c.4495A>C	XP_005269066.1:p.Ser1499Arg
XM_005269010.1:c.4477A>C	XP_005269067.1:p.Ser1493Arg
XM_005269010.3:c.4477A>C	XP_005269067.1:p.Ser1493Arg
XM_005269011.1:c.4462A>C	XP_005269068.1:p.Ser1488Arg
XM_005269011.3:c.4462A>C	XP_005269068.1:p.Ser1488Arg
XM_005269012.1:c.4387A>C	XP_005269069.1:p.Ser1463Arg
XM_005269012.3:c.4387A>C	XP_005269069.1:p.Ser1463Arg
XM_005269013.1:c.4372A>C	XP_005269070.1:p.Ser1458Arg
XM_005269013.3:c.4372A>C	XP_005269070.1:p.Ser1458Arg
XM_005269014.1:c.4333A>C	XP_005269071.1:p.Ser1445Arg
XM_005269014.3:c.4333A>C	XP_005269071.1:p.Ser1445Arg
XM_006719493.1:c.4456A>C	XP_006719556.1:p.Ser1486Arg
XM_006719493.3:c.4456A>C	XP_006719556.1:p.Ser1486Arg
XM_006719494.1:c.4384A>C	XP_006719557.1:p.Ser1462Arg
XM_006719494.3:c.4384A>C	XP_006719557.1:p.Ser1462Arg
XM_006719496.1:c.4441A>C	XP_006719559.1:p.Ser1481Arg
XM_011538556.1:c.4447A>C	XP_011536858.1:p.Ser1483Arg
XM_011538556.3:c.4447A>C	XP_011536858.1:p.Ser1483Arg
XM_017019607.2:c.4462A>C	XP_016875096.1:p.Ser1488Arg
XM_017019608.2:c.4423A>C	XP_016875097.1:p.Ser1475Arg
XM_017019609.2:c.4312A>C	XP_016875098.1:p.Ser1438Arg
XM_017019610.2:c.4312A>C	XP_016875099.1:p.Ser1438Arg
XM_017019611.2:c.4294A>C	XP_016875100.1:p.Ser1432Arg