Canonical Allele Identifier: CA384387113

Gene: KIF21A

Linked Data

• dbSNP Id: rs2137324478
• MyVariant Identifiers: chr12:g.39703451A>C (hg19) ; chr12:g.39309649A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309649A>C , CM000674.2:g.39309649A>C	GRCh38
NC_000012.11:g.39703451A>C , CM000674.1:g.39703451A>C	GRCh37
NC_000012.10:g.37989718A>C	NCBI36
NG_017067.1:g.138742T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4214T>G MANE Select	ENSP00000354878.5:p.Val1405Gly
ENST00000636569.1:c.4151T>G	ENSP00000490369.1:p.Val1384Gly
ENST00000361418.9:c.4214T>G	ENSP00000354878.5:p.Val1405Gly
ENST00000361961.7:c.4175T>G	ENSP00000354851.3:p.Val1392Gly
ENST00000541463.6:c.4055T>G	ENSP00000438075.2:p.Val1352Gly
ENST00000544797.6:c.4103T>G	ENSP00000445606.2:p.Val1368Gly
ENST00000547733.1:n.1528T>G
ENST00000551264.5:c.1157T>G	ENSP00000448792.1:p.Val386Gly
ENST00000552961.5:c.2116T>G
NM_001173463.1:c.4103T>G	NP_001166934.1:p.Val1368Gly
NM_001173464.1:c.4214T>G	NP_001166935.1:p.Val1405Gly
NM_001173465.1:c.4055T>G	NP_001166936.1:p.Val1352Gly
NM_017641.3:c.4175T>G	NP_060111.2:p.Val1392Gly
XM_005269007.1:c.4217T>G	XP_005269064.1:p.Val1406Gly
XM_005269008.1:c.4202T>G	XP_005269065.1:p.Val1401Gly
XM_005269009.1:c.4196T>G	XP_005269066.1:p.Val1399Gly
XM_005269010.1:c.4178T>G	XP_005269067.1:p.Val1393Gly
XM_005269011.1:c.4163T>G	XP_005269068.1:p.Val1388Gly
XM_005269012.1:c.4088T>G	XP_005269069.1:p.Val1363Gly
XM_005269013.1:c.4073T>G	XP_005269070.1:p.Val1358Gly
XM_005269014.1:c.4034T>G	XP_005269071.1:p.Val1345Gly
XM_006719493.1:c.4157T>G	XP_006719556.1:p.Val1386Gly
XM_006719494.1:c.4085T>G	XP_006719557.1:p.Val1362Gly
XM_006719496.1:c.4142T>G	XP_006719559.1:p.Val1381Gly
XM_011538556.1:c.4148T>G	XP_011536858.1:p.Val1383Gly
XM_005269007.3:c.4217T>G	XP_005269064.1:p.Val1406Gly
XM_005269008.3:c.4202T>G	XP_005269065.1:p.Val1401Gly
XM_005269009.3:c.4196T>G	XP_005269066.1:p.Val1399Gly
XM_005269010.3:c.4178T>G	XP_005269067.1:p.Val1393Gly
XM_005269011.3:c.4163T>G	XP_005269068.1:p.Val1388Gly
XM_005269012.3:c.4088T>G	XP_005269069.1:p.Val1363Gly
XM_005269013.3:c.4073T>G	XP_005269070.1:p.Val1358Gly
XM_005269014.3:c.4034T>G	XP_005269071.1:p.Val1345Gly
XM_006719493.3:c.4157T>G	XP_006719556.1:p.Val1386Gly
XM_006719494.3:c.4085T>G	XP_006719557.1:p.Val1362Gly
XM_011538556.3:c.4148T>G	XP_011536858.1:p.Val1383Gly
XM_017019607.2:c.4163T>G	XP_016875096.1:p.Val1388Gly
XM_017019608.2:c.4124T>G	XP_016875097.1:p.Val1375Gly
XM_017019609.2:c.4013T>G	XP_016875098.1:p.Val1338Gly
XM_017019610.2:c.4013T>G	XP_016875099.1:p.Val1338Gly
XM_017019611.2:c.3995T>G	XP_016875100.1:p.Val1332Gly
NM_001173463.2:c.4103T>G	NP_001166934.1:p.Val1368Gly
NM_001173464.2:c.4214T>G MANE Select	NP_001166935.1:p.Val1405Gly
NM_001173465.2:c.4055T>G	NP_001166936.1:p.Val1352Gly
NM_017641.4:c.4175T>G	NP_060111.2:p.Val1392Gly
NM_001378439.1:c.4217T>G	NP_001365368.1:p.Val1406Gly
NM_001378440.1:c.4202T>G	NP_001365369.1:p.Val1401Gly
NM_001378441.1:c.4178T>G	NP_001365370.1:p.Val1393Gly