Canonical Allele Identifier: CA384386782

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703399A>C (hg19) ; chr12:g.39309597A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309597A>C , CM000674.2:g.39309597A>C	GRCh38
NC_000012.11:g.39703399A>C , CM000674.1:g.39703399A>C	GRCh37
NC_000012.10:g.37989666A>C	NCBI36
NG_017067.1:g.138794T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000361418.10:c.4266T>G MANE Select	ENSP00000354878.5:p.Ile1422Met
ENST00000636569.1:c.4203T>G	ENSP00000490369.1:p.Ile1401Met
ENST00000361418.9:c.4266T>G	ENSP00000354878.5:p.Ile1422Met
ENST00000361961.7:c.4227T>G	ENSP00000354851.3:p.Ile1409Met
ENST00000541463.6:c.4107T>G	ENSP00000438075.2:p.Ile1369Met
ENST00000544797.6:c.4155T>G	ENSP00000445606.2:p.Ile1385Met
ENST00000547733.1:n.1580T>G
ENST00000551264.5:c.1209T>G	ENSP00000448792.1:p.Ile403Met
ENST00000552961.5:c.2168T>G
NM_001173463.1:c.4155T>G	NP_001166934.1:p.Ile1385Met
NM_001173464.1:c.4266T>G	NP_001166935.1:p.Ile1422Met
NM_001173465.1:c.4107T>G	NP_001166936.1:p.Ile1369Met
NM_017641.3:c.4227T>G	NP_060111.2:p.Ile1409Met
XM_005269007.1:c.4269T>G	XP_005269064.1:p.Ile1423Met
XM_005269008.1:c.4254T>G	XP_005269065.1:p.Ile1418Met
XM_005269009.1:c.4248T>G	XP_005269066.1:p.Ile1416Met
XM_005269010.1:c.4230T>G	XP_005269067.1:p.Ile1410Met
XM_005269011.1:c.4215T>G	XP_005269068.1:p.Ile1405Met
XM_005269012.1:c.4140T>G	XP_005269069.1:p.Ile1380Met
XM_005269013.1:c.4125T>G	XP_005269070.1:p.Ile1375Met
XM_005269014.1:c.4086T>G	XP_005269071.1:p.Ile1362Met
XM_006719493.1:c.4209T>G	XP_006719556.1:p.Ile1403Met
XM_006719494.1:c.4137T>G	XP_006719557.1:p.Ile1379Met
XM_006719496.1:c.4194T>G	XP_006719559.1:p.Ile1398Met
XM_011538556.1:c.4200T>G	XP_011536858.1:p.Ile1400Met
XM_005269007.3:c.4269T>G	XP_005269064.1:p.Ile1423Met
XM_005269008.3:c.4254T>G	XP_005269065.1:p.Ile1418Met
XM_005269009.3:c.4248T>G	XP_005269066.1:p.Ile1416Met
XM_005269010.3:c.4230T>G	XP_005269067.1:p.Ile1410Met
XM_005269011.3:c.4215T>G	XP_005269068.1:p.Ile1405Met
XM_005269012.3:c.4140T>G	XP_005269069.1:p.Ile1380Met
XM_005269013.3:c.4125T>G	XP_005269070.1:p.Ile1375Met
XM_005269014.3:c.4086T>G	XP_005269071.1:p.Ile1362Met
XM_006719493.3:c.4209T>G	XP_006719556.1:p.Ile1403Met
XM_006719494.3:c.4137T>G	XP_006719557.1:p.Ile1379Met
XM_011538556.3:c.4200T>G	XP_011536858.1:p.Ile1400Met
XM_017019607.2:c.4215T>G	XP_016875096.1:p.Ile1405Met
XM_017019608.2:c.4176T>G	XP_016875097.1:p.Ile1392Met
XM_017019609.2:c.4065T>G	XP_016875098.1:p.Ile1355Met
XM_017019610.2:c.4065T>G	XP_016875099.1:p.Ile1355Met
XM_017019611.2:c.4047T>G	XP_016875100.1:p.Ile1349Met
NM_001173463.2:c.4155T>G	NP_001166934.1:p.Ile1385Met
NM_001173464.2:c.4266T>G MANE Select	NP_001166935.1:p.Ile1422Met
NM_001173465.2:c.4107T>G	NP_001166936.1:p.Ile1369Met
NM_017641.4:c.4227T>G	NP_060111.2:p.Ile1409Met
NM_001378439.1:c.4269T>G	NP_001365368.1:p.Ile1423Met
NM_001378440.1:c.4254T>G	NP_001365369.1:p.Ile1418Met
NM_001378441.1:c.4230T>G	NP_001365370.1:p.Ile1410Met