Canonical Allele Identifier: CA6510240

Gene: KIF21A

Linked Data

• dbSNP Id: rs745549119
• ExAC: 12:39703499 T / C
• gnomAD v2: 12-39703499-T-C
• gnomAD v4: 12-39309697-T-C
• MyVariant Identifiers: chr12:g.39703499T>C (hg19) ; chr12:g.39309697T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309697T>C , CM000674.2:g.39309697T>C	GRCh38
NC_000012.11:g.39703499T>C , CM000674.1:g.39703499T>C	GRCh37
NC_000012.10:g.37989766T>C	NCBI36
NG_017067.1:g.138694A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4166A>G MANE Select	ENSP00000354878.5:p.Asn1389Ser
ENST00000636569.1:c.4103A>G	ENSP00000490369.1:p.Asn1368Ser
ENST00000361418.9:c.4166A>G	ENSP00000354878.5:p.Asn1389Ser
ENST00000361961.7:c.4127A>G	ENSP00000354851.3:p.Asn1376Ser
ENST00000541463.6:c.4007A>G	ENSP00000438075.2:p.Asn1336Ser
ENST00000544797.6:c.4055A>G	ENSP00000445606.2:p.Asn1352Ser
ENST00000547733.1:n.1480A>G
ENST00000551264.5:c.1109A>G	ENSP00000448792.1:p.Asn370Ser
ENST00000552961.5:c.2068A>G
NM_001173463.1:c.4055A>G	NP_001166934.1:p.Asn1352Ser
NM_001173464.1:c.4166A>G	NP_001166935.1:p.Asn1389Ser
NM_001173465.1:c.4007A>G	NP_001166936.1:p.Asn1336Ser
NM_017641.3:c.4127A>G	NP_060111.2:p.Asn1376Ser
XM_005269007.1:c.4169A>G	XP_005269064.1:p.Asn1390Ser
XM_005269008.1:c.4154A>G	XP_005269065.1:p.Asn1385Ser
XM_005269009.1:c.4148A>G	XP_005269066.1:p.Asn1383Ser
XM_005269010.1:c.4130A>G	XP_005269067.1:p.Asn1377Ser
XM_005269011.1:c.4115A>G	XP_005269068.1:p.Asn1372Ser
XM_005269012.1:c.4040A>G	XP_005269069.1:p.Asn1347Ser
XM_005269013.1:c.4025A>G	XP_005269070.1:p.Asn1342Ser
XM_005269014.1:c.3986A>G	XP_005269071.1:p.Asn1329Ser
XM_006719493.1:c.4109A>G	XP_006719556.1:p.Asn1370Ser
XM_006719494.1:c.4037A>G	XP_006719557.1:p.Asn1346Ser
XM_006719496.1:c.4094A>G	XP_006719559.1:p.Asn1365Ser
XM_011538556.1:c.4100A>G	XP_011536858.1:p.Asn1367Ser
XM_005269007.3:c.4169A>G	XP_005269064.1:p.Asn1390Ser
XM_005269008.3:c.4154A>G	XP_005269065.1:p.Asn1385Ser
XM_005269009.3:c.4148A>G	XP_005269066.1:p.Asn1383Ser
XM_005269010.3:c.4130A>G	XP_005269067.1:p.Asn1377Ser
XM_005269011.3:c.4115A>G	XP_005269068.1:p.Asn1372Ser
XM_005269012.3:c.4040A>G	XP_005269069.1:p.Asn1347Ser
XM_005269013.3:c.4025A>G	XP_005269070.1:p.Asn1342Ser
XM_005269014.3:c.3986A>G	XP_005269071.1:p.Asn1329Ser
XM_006719493.3:c.4109A>G	XP_006719556.1:p.Asn1370Ser
XM_006719494.3:c.4037A>G	XP_006719557.1:p.Asn1346Ser
XM_011538556.3:c.4100A>G	XP_011536858.1:p.Asn1367Ser
XM_017019607.2:c.4115A>G	XP_016875096.1:p.Asn1372Ser
XM_017019608.2:c.4076A>G	XP_016875097.1:p.Asn1359Ser
XM_017019609.2:c.3965A>G	XP_016875098.1:p.Asn1322Ser
XM_017019610.2:c.3965A>G	XP_016875099.1:p.Asn1322Ser
XM_017019611.2:c.3947A>G	XP_016875100.1:p.Asn1316Ser
NM_001173463.2:c.4055A>G	NP_001166934.1:p.Asn1352Ser
NM_001173464.2:c.4166A>G MANE Select	NP_001166935.1:p.Asn1389Ser
NM_001173465.2:c.4007A>G	NP_001166936.1:p.Asn1336Ser
NM_017641.4:c.4127A>G	NP_060111.2:p.Asn1376Ser
NM_001378439.1:c.4169A>G	NP_001365368.1:p.Asn1390Ser
NM_001378440.1:c.4154A>G	NP_001365369.1:p.Asn1385Ser
NM_001378441.1:c.4130A>G	NP_001365370.1:p.Asn1377Ser