Canonical Allele Identifier: CA479233407

Gene: KIF21A

Linked Data

• dbSNP Id: rs1473348076
• gnomAD v2: 12-39703480-G-A
• gnomAD v4: 12-39309678-G-A
• MyVariant Identifiers: chr12:g.39703480G>A (hg19) ; chr12:g.39309678G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309678G>A , CM000674.2:g.39309678G>A	GRCh38
NC_000012.11:g.39703480G>A , CM000674.1:g.39703480G>A	GRCh37
NC_000012.10:g.37989747G>A	NCBI36
NG_017067.1:g.138713C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4185C>T MANE Select	ENSP00000354878.5:p.Tyr1395=
ENST00000636569.1:c.4122C>T	ENSP00000490369.1:p.Tyr1374=
ENST00000361418.9:c.4185C>T	ENSP00000354878.5:p.Tyr1395=
ENST00000361961.7:c.4146C>T	ENSP00000354851.3:p.Tyr1382=
ENST00000541463.6:c.4026C>T	ENSP00000438075.2:p.Tyr1342=
ENST00000544797.6:c.4074C>T	ENSP00000445606.2:p.Tyr1358=
ENST00000547733.1:n.1499C>T
ENST00000551264.5:c.1128C>T	ENSP00000448792.1:p.Tyr376=
ENST00000552961.5:c.2087C>T
NM_001173463.1:c.4074C>T	NP_001166934.1:p.Tyr1358=
NM_001173464.1:c.4185C>T	NP_001166935.1:p.Tyr1395=
NM_001173465.1:c.4026C>T	NP_001166936.1:p.Tyr1342=
NM_017641.3:c.4146C>T	NP_060111.2:p.Tyr1382=
XM_005269007.1:c.4188C>T	XP_005269064.1:p.Tyr1396=
XM_005269008.1:c.4173C>T	XP_005269065.1:p.Tyr1391=
XM_005269009.1:c.4167C>T	XP_005269066.1:p.Tyr1389=
XM_005269010.1:c.4149C>T	XP_005269067.1:p.Tyr1383=
XM_005269011.1:c.4134C>T	XP_005269068.1:p.Tyr1378=
XM_005269012.1:c.4059C>T	XP_005269069.1:p.Tyr1353=
XM_005269013.1:c.4044C>T	XP_005269070.1:p.Tyr1348=
XM_005269014.1:c.4005C>T	XP_005269071.1:p.Tyr1335=
XM_006719493.1:c.4128C>T	XP_006719556.1:p.Tyr1376=
XM_006719494.1:c.4056C>T	XP_006719557.1:p.Tyr1352=
XM_006719496.1:c.4113C>T	XP_006719559.1:p.Tyr1371=
XM_011538556.1:c.4119C>T	XP_011536858.1:p.Tyr1373=
XM_005269007.3:c.4188C>T	XP_005269064.1:p.Tyr1396=
XM_005269008.3:c.4173C>T	XP_005269065.1:p.Tyr1391=
XM_005269009.3:c.4167C>T	XP_005269066.1:p.Tyr1389=
XM_005269010.3:c.4149C>T	XP_005269067.1:p.Tyr1383=
XM_005269011.3:c.4134C>T	XP_005269068.1:p.Tyr1378=
XM_005269012.3:c.4059C>T	XP_005269069.1:p.Tyr1353=
XM_005269013.3:c.4044C>T	XP_005269070.1:p.Tyr1348=
XM_005269014.3:c.4005C>T	XP_005269071.1:p.Tyr1335=
XM_006719493.3:c.4128C>T	XP_006719556.1:p.Tyr1376=
XM_006719494.3:c.4056C>T	XP_006719557.1:p.Tyr1352=
XM_011538556.3:c.4119C>T	XP_011536858.1:p.Tyr1373=
XM_017019607.2:c.4134C>T	XP_016875096.1:p.Tyr1378=
XM_017019608.2:c.4095C>T	XP_016875097.1:p.Tyr1365=
XM_017019609.2:c.3984C>T	XP_016875098.1:p.Tyr1328=
XM_017019610.2:c.3984C>T	XP_016875099.1:p.Tyr1328=
XM_017019611.2:c.3966C>T	XP_016875100.1:p.Tyr1322=
NM_001173463.2:c.4074C>T	NP_001166934.1:p.Tyr1358=
NM_001173464.2:c.4185C>T MANE Select	NP_001166935.1:p.Tyr1395=
NM_001173465.2:c.4026C>T	NP_001166936.1:p.Tyr1342=
NM_017641.4:c.4146C>T	NP_060111.2:p.Tyr1382=
NM_001378439.1:c.4188C>T	NP_001365368.1:p.Tyr1396=
NM_001378440.1:c.4173C>T	NP_001365369.1:p.Tyr1391=
NM_001378441.1:c.4149C>T	NP_001365370.1:p.Tyr1383=