Canonical Allele Identifier: CA384387240

Gene: KIF21A

Linked Data

• dbSNP Id: rs925281361
• gnomAD v2: 12-39703472-T-A
• gnomAD v4: 12-39309670-T-A
• MyVariant Identifiers: chr12:g.39703472T>A (hg19) ; chr12:g.39309670T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309670T>A , CM000674.2:g.39309670T>A	GRCh38
NC_000012.11:g.39703472T>A , CM000674.1:g.39703472T>A	GRCh37
NC_000012.10:g.37989739T>A	NCBI36
NG_017067.1:g.138721A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4193A>T MANE Select	ENSP00000354878.5:p.Tyr1398Phe
ENST00000636569.1:c.4130A>T	ENSP00000490369.1:p.Tyr1377Phe
ENST00000361418.9:c.4193A>T	ENSP00000354878.5:p.Tyr1398Phe
ENST00000361961.7:c.4154A>T	ENSP00000354851.3:p.Tyr1385Phe
ENST00000541463.6:c.4034A>T	ENSP00000438075.2:p.Tyr1345Phe
ENST00000544797.6:c.4082A>T	ENSP00000445606.2:p.Tyr1361Phe
ENST00000547733.1:n.1507A>T
ENST00000551264.5:c.1136A>T	ENSP00000448792.1:p.Tyr379Phe
ENST00000552961.5:c.2095A>T
NM_001173463.1:c.4082A>T	NP_001166934.1:p.Tyr1361Phe
NM_001173464.1:c.4193A>T	NP_001166935.1:p.Tyr1398Phe
NM_001173465.1:c.4034A>T	NP_001166936.1:p.Tyr1345Phe
NM_017641.3:c.4154A>T	NP_060111.2:p.Tyr1385Phe
XM_005269007.1:c.4196A>T	XP_005269064.1:p.Tyr1399Phe
XM_005269008.1:c.4181A>T	XP_005269065.1:p.Tyr1394Phe
XM_005269009.1:c.4175A>T	XP_005269066.1:p.Tyr1392Phe
XM_005269010.1:c.4157A>T	XP_005269067.1:p.Tyr1386Phe
XM_005269011.1:c.4142A>T	XP_005269068.1:p.Tyr1381Phe
XM_005269012.1:c.4067A>T	XP_005269069.1:p.Tyr1356Phe
XM_005269013.1:c.4052A>T	XP_005269070.1:p.Tyr1351Phe
XM_005269014.1:c.4013A>T	XP_005269071.1:p.Tyr1338Phe
XM_006719493.1:c.4136A>T	XP_006719556.1:p.Tyr1379Phe
XM_006719494.1:c.4064A>T	XP_006719557.1:p.Tyr1355Phe
XM_006719496.1:c.4121A>T	XP_006719559.1:p.Tyr1374Phe
XM_011538556.1:c.4127A>T	XP_011536858.1:p.Tyr1376Phe
XM_005269007.3:c.4196A>T	XP_005269064.1:p.Tyr1399Phe
XM_005269008.3:c.4181A>T	XP_005269065.1:p.Tyr1394Phe
XM_005269009.3:c.4175A>T	XP_005269066.1:p.Tyr1392Phe
XM_005269010.3:c.4157A>T	XP_005269067.1:p.Tyr1386Phe
XM_005269011.3:c.4142A>T	XP_005269068.1:p.Tyr1381Phe
XM_005269012.3:c.4067A>T	XP_005269069.1:p.Tyr1356Phe
XM_005269013.3:c.4052A>T	XP_005269070.1:p.Tyr1351Phe
XM_005269014.3:c.4013A>T	XP_005269071.1:p.Tyr1338Phe
XM_006719493.3:c.4136A>T	XP_006719556.1:p.Tyr1379Phe
XM_006719494.3:c.4064A>T	XP_006719557.1:p.Tyr1355Phe
XM_011538556.3:c.4127A>T	XP_011536858.1:p.Tyr1376Phe
XM_017019607.2:c.4142A>T	XP_016875096.1:p.Tyr1381Phe
XM_017019608.2:c.4103A>T	XP_016875097.1:p.Tyr1368Phe
XM_017019609.2:c.3992A>T	XP_016875098.1:p.Tyr1331Phe
XM_017019610.2:c.3992A>T	XP_016875099.1:p.Tyr1331Phe
XM_017019611.2:c.3974A>T	XP_016875100.1:p.Tyr1325Phe
NM_001173463.2:c.4082A>T	NP_001166934.1:p.Tyr1361Phe
NM_001173464.2:c.4193A>T MANE Select	NP_001166935.1:p.Tyr1398Phe
NM_001173465.2:c.4034A>T	NP_001166936.1:p.Tyr1345Phe
NM_017641.4:c.4154A>T	NP_060111.2:p.Tyr1385Phe
NM_001378439.1:c.4196A>T	NP_001365368.1:p.Tyr1399Phe
NM_001378440.1:c.4181A>T	NP_001365369.1:p.Tyr1394Phe
NM_001378441.1:c.4157A>T	NP_001365370.1:p.Tyr1386Phe