Canonical Allele Identifier: CA384387237

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703471A>T (hg19) ; chr12:g.39309669A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309669A>T , CM000674.2:g.39309669A>T	GRCh38
NC_000012.11:g.39703471A>T , CM000674.1:g.39703471A>T	GRCh37
NC_000012.10:g.37989738A>T	NCBI36
NG_017067.1:g.138722T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4194T>A MANE Select	ENSP00000354878.5:p.Tyr1398Ter
ENST00000636569.1:c.4131T>A	ENSP00000490369.1:p.Tyr1377Ter
ENST00000361418.9:c.4194T>A	ENSP00000354878.5:p.Tyr1398Ter
ENST00000361961.7:c.4155T>A	ENSP00000354851.3:p.Tyr1385Ter
ENST00000541463.6:c.4035T>A	ENSP00000438075.2:p.Tyr1345Ter
ENST00000544797.6:c.4083T>A	ENSP00000445606.2:p.Tyr1361Ter
ENST00000547733.1:n.1508T>A
ENST00000551264.5:c.1137T>A	ENSP00000448792.1:p.Tyr379Ter
ENST00000552961.5:c.2096T>A
NM_001173463.1:c.4083T>A	NP_001166934.1:p.Tyr1361Ter
NM_001173464.1:c.4194T>A	NP_001166935.1:p.Tyr1398Ter
NM_001173465.1:c.4035T>A	NP_001166936.1:p.Tyr1345Ter
NM_017641.3:c.4155T>A	NP_060111.2:p.Tyr1385Ter
XM_005269007.1:c.4197T>A	XP_005269064.1:p.Tyr1399Ter
XM_005269008.1:c.4182T>A	XP_005269065.1:p.Tyr1394Ter
XM_005269009.1:c.4176T>A	XP_005269066.1:p.Tyr1392Ter
XM_005269010.1:c.4158T>A	XP_005269067.1:p.Tyr1386Ter
XM_005269011.1:c.4143T>A	XP_005269068.1:p.Tyr1381Ter
XM_005269012.1:c.4068T>A	XP_005269069.1:p.Tyr1356Ter
XM_005269013.1:c.4053T>A	XP_005269070.1:p.Tyr1351Ter
XM_005269014.1:c.4014T>A	XP_005269071.1:p.Tyr1338Ter
XM_006719493.1:c.4137T>A	XP_006719556.1:p.Tyr1379Ter
XM_006719494.1:c.4065T>A	XP_006719557.1:p.Tyr1355Ter
XM_006719496.1:c.4122T>A	XP_006719559.1:p.Tyr1374Ter
XM_011538556.1:c.4128T>A	XP_011536858.1:p.Tyr1376Ter
XM_005269007.3:c.4197T>A	XP_005269064.1:p.Tyr1399Ter
XM_005269008.3:c.4182T>A	XP_005269065.1:p.Tyr1394Ter
XM_005269009.3:c.4176T>A	XP_005269066.1:p.Tyr1392Ter
XM_005269010.3:c.4158T>A	XP_005269067.1:p.Tyr1386Ter
XM_005269011.3:c.4143T>A	XP_005269068.1:p.Tyr1381Ter
XM_005269012.3:c.4068T>A	XP_005269069.1:p.Tyr1356Ter
XM_005269013.3:c.4053T>A	XP_005269070.1:p.Tyr1351Ter
XM_005269014.3:c.4014T>A	XP_005269071.1:p.Tyr1338Ter
XM_006719493.3:c.4137T>A	XP_006719556.1:p.Tyr1379Ter
XM_006719494.3:c.4065T>A	XP_006719557.1:p.Tyr1355Ter
XM_011538556.3:c.4128T>A	XP_011536858.1:p.Tyr1376Ter
XM_017019607.2:c.4143T>A	XP_016875096.1:p.Tyr1381Ter
XM_017019608.2:c.4104T>A	XP_016875097.1:p.Tyr1368Ter
XM_017019609.2:c.3993T>A	XP_016875098.1:p.Tyr1331Ter
XM_017019610.2:c.3993T>A	XP_016875099.1:p.Tyr1331Ter
XM_017019611.2:c.3975T>A	XP_016875100.1:p.Tyr1325Ter
NM_001173463.2:c.4083T>A	NP_001166934.1:p.Tyr1361Ter
NM_001173464.2:c.4194T>A MANE Select	NP_001166935.1:p.Tyr1398Ter
NM_001173465.2:c.4035T>A	NP_001166936.1:p.Tyr1345Ter
NM_017641.4:c.4155T>A	NP_060111.2:p.Tyr1385Ter
NM_001378439.1:c.4197T>A	NP_001365368.1:p.Tyr1399Ter
NM_001378440.1:c.4182T>A	NP_001365369.1:p.Tyr1394Ter
NM_001378441.1:c.4158T>A	NP_001365370.1:p.Tyr1386Ter