Canonical Allele Identifier: CA384387251

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703473A>C (hg19) ; chr12:g.39309671A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309671A>C , CM000674.2:g.39309671A>C	GRCh38
NC_000012.11:g.39703473A>C , CM000674.1:g.39703473A>C	GRCh37
NC_000012.10:g.37989740A>C	NCBI36
NG_017067.1:g.138720T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4192T>G MANE Select	ENSP00000354878.5:p.Tyr1398Asp
ENST00000636569.1:c.4129T>G	ENSP00000490369.1:p.Tyr1377Asp
ENST00000361418.9:c.4192T>G	ENSP00000354878.5:p.Tyr1398Asp
ENST00000361961.7:c.4153T>G	ENSP00000354851.3:p.Tyr1385Asp
ENST00000541463.6:c.4033T>G	ENSP00000438075.2:p.Tyr1345Asp
ENST00000544797.6:c.4081T>G	ENSP00000445606.2:p.Tyr1361Asp
ENST00000547733.1:n.1506T>G
ENST00000551264.5:c.1135T>G	ENSP00000448792.1:p.Tyr379Asp
ENST00000552961.5:c.2094T>G
NM_001173463.1:c.4081T>G	NP_001166934.1:p.Tyr1361Asp
NM_001173464.1:c.4192T>G	NP_001166935.1:p.Tyr1398Asp
NM_001173465.1:c.4033T>G	NP_001166936.1:p.Tyr1345Asp
NM_017641.3:c.4153T>G	NP_060111.2:p.Tyr1385Asp
XM_005269007.1:c.4195T>G	XP_005269064.1:p.Tyr1399Asp
XM_005269008.1:c.4180T>G	XP_005269065.1:p.Tyr1394Asp
XM_005269009.1:c.4174T>G	XP_005269066.1:p.Tyr1392Asp
XM_005269010.1:c.4156T>G	XP_005269067.1:p.Tyr1386Asp
XM_005269011.1:c.4141T>G	XP_005269068.1:p.Tyr1381Asp
XM_005269012.1:c.4066T>G	XP_005269069.1:p.Tyr1356Asp
XM_005269013.1:c.4051T>G	XP_005269070.1:p.Tyr1351Asp
XM_005269014.1:c.4012T>G	XP_005269071.1:p.Tyr1338Asp
XM_006719493.1:c.4135T>G	XP_006719556.1:p.Tyr1379Asp
XM_006719494.1:c.4063T>G	XP_006719557.1:p.Tyr1355Asp
XM_006719496.1:c.4120T>G	XP_006719559.1:p.Tyr1374Asp
XM_011538556.1:c.4126T>G	XP_011536858.1:p.Tyr1376Asp
XM_005269007.3:c.4195T>G	XP_005269064.1:p.Tyr1399Asp
XM_005269008.3:c.4180T>G	XP_005269065.1:p.Tyr1394Asp
XM_005269009.3:c.4174T>G	XP_005269066.1:p.Tyr1392Asp
XM_005269010.3:c.4156T>G	XP_005269067.1:p.Tyr1386Asp
XM_005269011.3:c.4141T>G	XP_005269068.1:p.Tyr1381Asp
XM_005269012.3:c.4066T>G	XP_005269069.1:p.Tyr1356Asp
XM_005269013.3:c.4051T>G	XP_005269070.1:p.Tyr1351Asp
XM_005269014.3:c.4012T>G	XP_005269071.1:p.Tyr1338Asp
XM_006719493.3:c.4135T>G	XP_006719556.1:p.Tyr1379Asp
XM_006719494.3:c.4063T>G	XP_006719557.1:p.Tyr1355Asp
XM_011538556.3:c.4126T>G	XP_011536858.1:p.Tyr1376Asp
XM_017019607.2:c.4141T>G	XP_016875096.1:p.Tyr1381Asp
XM_017019608.2:c.4102T>G	XP_016875097.1:p.Tyr1368Asp
XM_017019609.2:c.3991T>G	XP_016875098.1:p.Tyr1331Asp
XM_017019610.2:c.3991T>G	XP_016875099.1:p.Tyr1331Asp
XM_017019611.2:c.3973T>G	XP_016875100.1:p.Tyr1325Asp
NM_001173463.2:c.4081T>G	NP_001166934.1:p.Tyr1361Asp
NM_001173464.2:c.4192T>G MANE Select	NP_001166935.1:p.Tyr1398Asp
NM_001173465.2:c.4033T>G	NP_001166936.1:p.Tyr1345Asp
NM_017641.4:c.4153T>G	NP_060111.2:p.Tyr1385Asp
NM_001378439.1:c.4195T>G	NP_001365368.1:p.Tyr1399Asp
NM_001378440.1:c.4180T>G	NP_001365369.1:p.Tyr1394Asp
NM_001378441.1:c.4156T>G	NP_001365370.1:p.Tyr1386Asp