Canonical Allele Identifier: CA384387015

Gene: KIF21A

Linked Data

• gnomAD v4: 12-39309632-T-C
• MyVariant Identifiers: chr12:g.39703434T>C (hg19) ; chr12:g.39309632T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309632T>C , CM000674.2:g.39309632T>C	GRCh38
NC_000012.11:g.39703434T>C , CM000674.1:g.39703434T>C	GRCh37
NC_000012.10:g.37989701T>C	NCBI36
NG_017067.1:g.138759A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4231A>G MANE Select	ENSP00000354878.5:p.Lys1411Glu
ENST00000636569.1:c.4168A>G	ENSP00000490369.1:p.Lys1390Glu
ENST00000361418.9:c.4231A>G	ENSP00000354878.5:p.Lys1411Glu
ENST00000361961.7:c.4192A>G	ENSP00000354851.3:p.Lys1398Glu
ENST00000541463.6:c.4072A>G	ENSP00000438075.2:p.Lys1358Glu
ENST00000544797.6:c.4120A>G	ENSP00000445606.2:p.Lys1374Glu
ENST00000547733.1:n.1545A>G
ENST00000551264.5:c.1174A>G	ENSP00000448792.1:p.Lys392Glu
ENST00000552961.5:c.2133A>G
NM_001173463.1:c.4120A>G	NP_001166934.1:p.Lys1374Glu
NM_001173464.1:c.4231A>G	NP_001166935.1:p.Lys1411Glu
NM_001173465.1:c.4072A>G	NP_001166936.1:p.Lys1358Glu
NM_017641.3:c.4192A>G	NP_060111.2:p.Lys1398Glu
XM_005269007.1:c.4234A>G	XP_005269064.1:p.Lys1412Glu
XM_005269008.1:c.4219A>G	XP_005269065.1:p.Lys1407Glu
XM_005269009.1:c.4213A>G	XP_005269066.1:p.Lys1405Glu
XM_005269010.1:c.4195A>G	XP_005269067.1:p.Lys1399Glu
XM_005269011.1:c.4180A>G	XP_005269068.1:p.Lys1394Glu
XM_005269012.1:c.4105A>G	XP_005269069.1:p.Lys1369Glu
XM_005269013.1:c.4090A>G	XP_005269070.1:p.Lys1364Glu
XM_005269014.1:c.4051A>G	XP_005269071.1:p.Lys1351Glu
XM_006719493.1:c.4174A>G	XP_006719556.1:p.Lys1392Glu
XM_006719494.1:c.4102A>G	XP_006719557.1:p.Lys1368Glu
XM_006719496.1:c.4159A>G	XP_006719559.1:p.Lys1387Glu
XM_011538556.1:c.4165A>G	XP_011536858.1:p.Lys1389Glu
XM_005269007.3:c.4234A>G	XP_005269064.1:p.Lys1412Glu
XM_005269008.3:c.4219A>G	XP_005269065.1:p.Lys1407Glu
XM_005269009.3:c.4213A>G	XP_005269066.1:p.Lys1405Glu
XM_005269010.3:c.4195A>G	XP_005269067.1:p.Lys1399Glu
XM_005269011.3:c.4180A>G	XP_005269068.1:p.Lys1394Glu
XM_005269012.3:c.4105A>G	XP_005269069.1:p.Lys1369Glu
XM_005269013.3:c.4090A>G	XP_005269070.1:p.Lys1364Glu
XM_005269014.3:c.4051A>G	XP_005269071.1:p.Lys1351Glu
XM_006719493.3:c.4174A>G	XP_006719556.1:p.Lys1392Glu
XM_006719494.3:c.4102A>G	XP_006719557.1:p.Lys1368Glu
XM_011538556.3:c.4165A>G	XP_011536858.1:p.Lys1389Glu
XM_017019607.2:c.4180A>G	XP_016875096.1:p.Lys1394Glu
XM_017019608.2:c.4141A>G	XP_016875097.1:p.Lys1381Glu
XM_017019609.2:c.4030A>G	XP_016875098.1:p.Lys1344Glu
XM_017019610.2:c.4030A>G	XP_016875099.1:p.Lys1344Glu
XM_017019611.2:c.4012A>G	XP_016875100.1:p.Lys1338Glu
NM_001173463.2:c.4120A>G	NP_001166934.1:p.Lys1374Glu
NM_001173464.2:c.4231A>G MANE Select	NP_001166935.1:p.Lys1411Glu
NM_001173465.2:c.4072A>G	NP_001166936.1:p.Lys1358Glu
NM_017641.4:c.4192A>G	NP_060111.2:p.Lys1398Glu
NM_001378439.1:c.4234A>G	NP_001365368.1:p.Lys1412Glu
NM_001378440.1:c.4219A>G	NP_001365369.1:p.Lys1407Glu
NM_001378441.1:c.4195A>G	NP_001365370.1:p.Lys1399Glu