Canonical Allele Identifier: CA384387125

Gene: KIF21A

Linked Data

• dbSNP Id: rs1344148767
• gnomAD v2: 12-39703454-G-C
• gnomAD v3: 12-39309652-G-C
• gnomAD v4: 12-39309652-G-C
• MyVariant Identifiers: chr12:g.39703454G>C (hg19) ; chr12:g.39309652G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309652G>C , CM000674.2:g.39309652G>C	GRCh38
NC_000012.11:g.39703454G>C , CM000674.1:g.39703454G>C	GRCh37
NC_000012.10:g.37989721G>C	NCBI36
NG_017067.1:g.138739C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4211C>G MANE Select	ENSP00000354878.5:p.Thr1404Ser
ENST00000636569.1:c.4148C>G	ENSP00000490369.1:p.Thr1383Ser
ENST00000361418.9:c.4211C>G	ENSP00000354878.5:p.Thr1404Ser
ENST00000361961.7:c.4172C>G	ENSP00000354851.3:p.Thr1391Ser
ENST00000541463.6:c.4052C>G	ENSP00000438075.2:p.Thr1351Ser
ENST00000544797.6:c.4100C>G	ENSP00000445606.2:p.Thr1367Ser
ENST00000547733.1:n.1525C>G
ENST00000551264.5:c.1154C>G	ENSP00000448792.1:p.Thr385Ser
ENST00000552961.5:c.2113C>G
NM_001173463.1:c.4100C>G	NP_001166934.1:p.Thr1367Ser
NM_001173464.1:c.4211C>G	NP_001166935.1:p.Thr1404Ser
NM_001173465.1:c.4052C>G	NP_001166936.1:p.Thr1351Ser
NM_017641.3:c.4172C>G	NP_060111.2:p.Thr1391Ser
XM_005269007.1:c.4214C>G	XP_005269064.1:p.Thr1405Ser
XM_005269008.1:c.4199C>G	XP_005269065.1:p.Thr1400Ser
XM_005269009.1:c.4193C>G	XP_005269066.1:p.Thr1398Ser
XM_005269010.1:c.4175C>G	XP_005269067.1:p.Thr1392Ser
XM_005269011.1:c.4160C>G	XP_005269068.1:p.Thr1387Ser
XM_005269012.1:c.4085C>G	XP_005269069.1:p.Thr1362Ser
XM_005269013.1:c.4070C>G	XP_005269070.1:p.Thr1357Ser
XM_005269014.1:c.4031C>G	XP_005269071.1:p.Thr1344Ser
XM_006719493.1:c.4154C>G	XP_006719556.1:p.Thr1385Ser
XM_006719494.1:c.4082C>G	XP_006719557.1:p.Thr1361Ser
XM_006719496.1:c.4139C>G	XP_006719559.1:p.Thr1380Ser
XM_011538556.1:c.4145C>G	XP_011536858.1:p.Thr1382Ser
XM_005269007.3:c.4214C>G	XP_005269064.1:p.Thr1405Ser
XM_005269008.3:c.4199C>G	XP_005269065.1:p.Thr1400Ser
XM_005269009.3:c.4193C>G	XP_005269066.1:p.Thr1398Ser
XM_005269010.3:c.4175C>G	XP_005269067.1:p.Thr1392Ser
XM_005269011.3:c.4160C>G	XP_005269068.1:p.Thr1387Ser
XM_005269012.3:c.4085C>G	XP_005269069.1:p.Thr1362Ser
XM_005269013.3:c.4070C>G	XP_005269070.1:p.Thr1357Ser
XM_005269014.3:c.4031C>G	XP_005269071.1:p.Thr1344Ser
XM_006719493.3:c.4154C>G	XP_006719556.1:p.Thr1385Ser
XM_006719494.3:c.4082C>G	XP_006719557.1:p.Thr1361Ser
XM_011538556.3:c.4145C>G	XP_011536858.1:p.Thr1382Ser
XM_017019607.2:c.4160C>G	XP_016875096.1:p.Thr1387Ser
XM_017019608.2:c.4121C>G	XP_016875097.1:p.Thr1374Ser
XM_017019609.2:c.4010C>G	XP_016875098.1:p.Thr1337Ser
XM_017019610.2:c.4010C>G	XP_016875099.1:p.Thr1337Ser
XM_017019611.2:c.3992C>G	XP_016875100.1:p.Thr1331Ser
NM_001173463.2:c.4100C>G	NP_001166934.1:p.Thr1367Ser
NM_001173464.2:c.4211C>G MANE Select	NP_001166935.1:p.Thr1404Ser
NM_001173465.2:c.4052C>G	NP_001166936.1:p.Thr1351Ser
NM_017641.4:c.4172C>G	NP_060111.2:p.Thr1391Ser
NM_001378439.1:c.4214C>G	NP_001365368.1:p.Thr1405Ser
NM_001378440.1:c.4199C>G	NP_001365369.1:p.Thr1400Ser
NM_001378441.1:c.4175C>G	NP_001365370.1:p.Thr1392Ser