Canonical Allele Identifier: CA479233418

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703495G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309693G>C , CM000674.2:g.39309693G>C	GRCh38
NC_000012.11:g.39703495G>C , CM000674.1:g.39703495G>C	GRCh37
NC_000012.10:g.37989762G>C	NCBI36
NG_017067.1:g.138698C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4170C>G MANE Select	ENSP00000354878.5:p.Val1390=
ENST00000636569.1:c.4107C>G	ENSP00000490369.1:p.Val1369=
ENST00000361418.9:c.4170C>G	ENSP00000354878.5:p.Val1390=
ENST00000361961.7:c.4131C>G	ENSP00000354851.3:p.Val1377=
ENST00000541463.6:c.4011C>G	ENSP00000438075.2:p.Val1337=
ENST00000544797.6:c.4059C>G	ENSP00000445606.2:p.Val1353=
ENST00000547733.1:n.1484C>G
ENST00000551264.5:c.1113C>G	ENSP00000448792.1:p.Val371=
ENST00000552961.5:c.2072C>G
NM_001173463.1:c.4059C>G	NP_001166934.1:p.Val1353=
NM_001173464.1:c.4170C>G	NP_001166935.1:p.Val1390=
NM_001173465.1:c.4011C>G	NP_001166936.1:p.Val1337=
NM_017641.3:c.4131C>G	NP_060111.2:p.Val1377=
XM_005269007.1:c.4173C>G	XP_005269064.1:p.Val1391=
XM_005269008.1:c.4158C>G	XP_005269065.1:p.Val1386=
XM_005269009.1:c.4152C>G	XP_005269066.1:p.Val1384=
XM_005269010.1:c.4134C>G	XP_005269067.1:p.Val1378=
XM_005269011.1:c.4119C>G	XP_005269068.1:p.Val1373=
XM_005269012.1:c.4044C>G	XP_005269069.1:p.Val1348=
XM_005269013.1:c.4029C>G	XP_005269070.1:p.Val1343=
XM_005269014.1:c.3990C>G	XP_005269071.1:p.Val1330=
XM_006719493.1:c.4113C>G	XP_006719556.1:p.Val1371=
XM_006719494.1:c.4041C>G	XP_006719557.1:p.Val1347=
XM_006719496.1:c.4098C>G	XP_006719559.1:p.Val1366=
XM_011538556.1:c.4104C>G	XP_011536858.1:p.Val1368=
XM_005269007.3:c.4173C>G	XP_005269064.1:p.Val1391=
XM_005269008.3:c.4158C>G	XP_005269065.1:p.Val1386=
XM_005269009.3:c.4152C>G	XP_005269066.1:p.Val1384=
XM_005269010.3:c.4134C>G	XP_005269067.1:p.Val1378=
XM_005269011.3:c.4119C>G	XP_005269068.1:p.Val1373=
XM_005269012.3:c.4044C>G	XP_005269069.1:p.Val1348=
XM_005269013.3:c.4029C>G	XP_005269070.1:p.Val1343=
XM_005269014.3:c.3990C>G	XP_005269071.1:p.Val1330=
XM_006719493.3:c.4113C>G	XP_006719556.1:p.Val1371=
XM_006719494.3:c.4041C>G	XP_006719557.1:p.Val1347=
XM_011538556.3:c.4104C>G	XP_011536858.1:p.Val1368=
XM_017019607.2:c.4119C>G	XP_016875096.1:p.Val1373=
XM_017019608.2:c.4080C>G	XP_016875097.1:p.Val1360=
XM_017019609.2:c.3969C>G	XP_016875098.1:p.Val1323=
XM_017019610.2:c.3969C>G	XP_016875099.1:p.Val1323=
XM_017019611.2:c.3951C>G	XP_016875100.1:p.Val1317=
NM_001173463.2:c.4059C>G	NP_001166934.1:p.Val1353=
NM_001173464.2:c.4170C>G MANE Select	NP_001166935.1:p.Val1390=
NM_001173465.2:c.4011C>G	NP_001166936.1:p.Val1337=
NM_017641.4:c.4131C>G	NP_060111.2:p.Val1377=
NM_001378439.1:c.4173C>G	NP_001365368.1:p.Val1391=
NM_001378440.1:c.4158C>G	NP_001365369.1:p.Val1386=
NM_001378441.1:c.4134C>G	NP_001365370.1:p.Val1378=