Canonical Allele Identifier: CA384386929

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703423A>C (hg19) ; chr12:g.39309621A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309621A>C , CM000674.2:g.39309621A>C	GRCh38
NC_000012.11:g.39703423A>C , CM000674.1:g.39703423A>C	GRCh37
NC_000012.10:g.37989690A>C	NCBI36
NG_017067.1:g.138770T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4242T>G MANE Select	ENSP00000354878.5:p.Asp1414Glu
ENST00000636569.1:c.4179T>G	ENSP00000490369.1:p.Asp1393Glu
ENST00000361418.9:c.4242T>G	ENSP00000354878.5:p.Asp1414Glu
ENST00000361961.7:c.4203T>G	ENSP00000354851.3:p.Asp1401Glu
ENST00000541463.6:c.4083T>G	ENSP00000438075.2:p.Asp1361Glu
ENST00000544797.6:c.4131T>G	ENSP00000445606.2:p.Asp1377Glu
ENST00000547733.1:n.1556T>G
ENST00000551264.5:c.1185T>G	ENSP00000448792.1:p.Asp395Glu
ENST00000552961.5:c.2144T>G
NM_001173463.1:c.4131T>G	NP_001166934.1:p.Asp1377Glu
NM_001173464.1:c.4242T>G	NP_001166935.1:p.Asp1414Glu
NM_001173465.1:c.4083T>G	NP_001166936.1:p.Asp1361Glu
NM_017641.3:c.4203T>G	NP_060111.2:p.Asp1401Glu
XM_005269007.1:c.4245T>G	XP_005269064.1:p.Asp1415Glu
XM_005269008.1:c.4230T>G	XP_005269065.1:p.Asp1410Glu
XM_005269009.1:c.4224T>G	XP_005269066.1:p.Asp1408Glu
XM_005269010.1:c.4206T>G	XP_005269067.1:p.Asp1402Glu
XM_005269011.1:c.4191T>G	XP_005269068.1:p.Asp1397Glu
XM_005269012.1:c.4116T>G	XP_005269069.1:p.Asp1372Glu
XM_005269013.1:c.4101T>G	XP_005269070.1:p.Asp1367Glu
XM_005269014.1:c.4062T>G	XP_005269071.1:p.Asp1354Glu
XM_006719493.1:c.4185T>G	XP_006719556.1:p.Asp1395Glu
XM_006719494.1:c.4113T>G	XP_006719557.1:p.Asp1371Glu
XM_006719496.1:c.4170T>G	XP_006719559.1:p.Asp1390Glu
XM_011538556.1:c.4176T>G	XP_011536858.1:p.Asp1392Glu
XM_005269007.3:c.4245T>G	XP_005269064.1:p.Asp1415Glu
XM_005269008.3:c.4230T>G	XP_005269065.1:p.Asp1410Glu
XM_005269009.3:c.4224T>G	XP_005269066.1:p.Asp1408Glu
XM_005269010.3:c.4206T>G	XP_005269067.1:p.Asp1402Glu
XM_005269011.3:c.4191T>G	XP_005269068.1:p.Asp1397Glu
XM_005269012.3:c.4116T>G	XP_005269069.1:p.Asp1372Glu
XM_005269013.3:c.4101T>G	XP_005269070.1:p.Asp1367Glu
XM_005269014.3:c.4062T>G	XP_005269071.1:p.Asp1354Glu
XM_006719493.3:c.4185T>G	XP_006719556.1:p.Asp1395Glu
XM_006719494.3:c.4113T>G	XP_006719557.1:p.Asp1371Glu
XM_011538556.3:c.4176T>G	XP_011536858.1:p.Asp1392Glu
XM_017019607.2:c.4191T>G	XP_016875096.1:p.Asp1397Glu
XM_017019608.2:c.4152T>G	XP_016875097.1:p.Asp1384Glu
XM_017019609.2:c.4041T>G	XP_016875098.1:p.Asp1347Glu
XM_017019610.2:c.4041T>G	XP_016875099.1:p.Asp1347Glu
XM_017019611.2:c.4023T>G	XP_016875100.1:p.Asp1341Glu
NM_001173463.2:c.4131T>G	NP_001166934.1:p.Asp1377Glu
NM_001173464.2:c.4242T>G MANE Select	NP_001166935.1:p.Asp1414Glu
NM_001173465.2:c.4083T>G	NP_001166936.1:p.Asp1361Glu
NM_017641.4:c.4203T>G	NP_060111.2:p.Asp1401Glu
NM_001378439.1:c.4245T>G	NP_001365368.1:p.Asp1415Glu
NM_001378440.1:c.4230T>G	NP_001365369.1:p.Asp1410Glu
NM_001378441.1:c.4206T>G	NP_001365370.1:p.Asp1402Glu