Canonical Allele Identifier: CA384387422

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703498A>C (hg19) ; chr12:g.39309696A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309696A>C , CM000674.2:g.39309696A>C	GRCh38
NC_000012.11:g.39703498A>C , CM000674.1:g.39703498A>C	GRCh37
NC_000012.10:g.37989765A>C	NCBI36
NG_017067.1:g.138695T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4167T>G MANE Select	ENSP00000354878.5:p.Asn1389Lys
ENST00000636569.1:c.4104T>G	ENSP00000490369.1:p.Asn1368Lys
ENST00000361418.9:c.4167T>G	ENSP00000354878.5:p.Asn1389Lys
ENST00000361961.7:c.4128T>G	ENSP00000354851.3:p.Asn1376Lys
ENST00000541463.6:c.4008T>G	ENSP00000438075.2:p.Asn1336Lys
ENST00000544797.6:c.4056T>G	ENSP00000445606.2:p.Asn1352Lys
ENST00000547733.1:n.1481T>G
ENST00000551264.5:c.1110T>G	ENSP00000448792.1:p.Asn370Lys
ENST00000552961.5:c.2069T>G
NM_001173463.1:c.4056T>G	NP_001166934.1:p.Asn1352Lys
NM_001173464.1:c.4167T>G	NP_001166935.1:p.Asn1389Lys
NM_001173465.1:c.4008T>G	NP_001166936.1:p.Asn1336Lys
NM_017641.3:c.4128T>G	NP_060111.2:p.Asn1376Lys
XM_005269007.1:c.4170T>G	XP_005269064.1:p.Asn1390Lys
XM_005269008.1:c.4155T>G	XP_005269065.1:p.Asn1385Lys
XM_005269009.1:c.4149T>G	XP_005269066.1:p.Asn1383Lys
XM_005269010.1:c.4131T>G	XP_005269067.1:p.Asn1377Lys
XM_005269011.1:c.4116T>G	XP_005269068.1:p.Asn1372Lys
XM_005269012.1:c.4041T>G	XP_005269069.1:p.Asn1347Lys
XM_005269013.1:c.4026T>G	XP_005269070.1:p.Asn1342Lys
XM_005269014.1:c.3987T>G	XP_005269071.1:p.Asn1329Lys
XM_006719493.1:c.4110T>G	XP_006719556.1:p.Asn1370Lys
XM_006719494.1:c.4038T>G	XP_006719557.1:p.Asn1346Lys
XM_006719496.1:c.4095T>G	XP_006719559.1:p.Asn1365Lys
XM_011538556.1:c.4101T>G	XP_011536858.1:p.Asn1367Lys
XM_005269007.3:c.4170T>G	XP_005269064.1:p.Asn1390Lys
XM_005269008.3:c.4155T>G	XP_005269065.1:p.Asn1385Lys
XM_005269009.3:c.4149T>G	XP_005269066.1:p.Asn1383Lys
XM_005269010.3:c.4131T>G	XP_005269067.1:p.Asn1377Lys
XM_005269011.3:c.4116T>G	XP_005269068.1:p.Asn1372Lys
XM_005269012.3:c.4041T>G	XP_005269069.1:p.Asn1347Lys
XM_005269013.3:c.4026T>G	XP_005269070.1:p.Asn1342Lys
XM_005269014.3:c.3987T>G	XP_005269071.1:p.Asn1329Lys
XM_006719493.3:c.4110T>G	XP_006719556.1:p.Asn1370Lys
XM_006719494.3:c.4038T>G	XP_006719557.1:p.Asn1346Lys
XM_011538556.3:c.4101T>G	XP_011536858.1:p.Asn1367Lys
XM_017019607.2:c.4116T>G	XP_016875096.1:p.Asn1372Lys
XM_017019608.2:c.4077T>G	XP_016875097.1:p.Asn1359Lys
XM_017019609.2:c.3966T>G	XP_016875098.1:p.Asn1322Lys
XM_017019610.2:c.3966T>G	XP_016875099.1:p.Asn1322Lys
XM_017019611.2:c.3948T>G	XP_016875100.1:p.Asn1316Lys
NM_001173463.2:c.4056T>G	NP_001166934.1:p.Asn1352Lys
NM_001173464.2:c.4167T>G MANE Select	NP_001166935.1:p.Asn1389Lys
NM_001173465.2:c.4008T>G	NP_001166936.1:p.Asn1336Lys
NM_017641.4:c.4128T>G	NP_060111.2:p.Asn1376Lys
NM_001378439.1:c.4170T>G	NP_001365368.1:p.Asn1390Lys
NM_001378440.1:c.4155T>G	NP_001365369.1:p.Asn1385Lys
NM_001378441.1:c.4131T>G	NP_001365370.1:p.Asn1377Lys