Canonical Allele Identifier: CA384386985

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703430A>G (hg19) ; chr12:g.39309628A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309628A>G , CM000674.2:g.39309628A>G	GRCh38
NC_000012.11:g.39703430A>G , CM000674.1:g.39703430A>G	GRCh37
NC_000012.10:g.37989697A>G	NCBI36
NG_017067.1:g.138763T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4235T>C MANE Select	ENSP00000354878.5:p.Val1412Ala
ENST00000636569.1:c.4172T>C	ENSP00000490369.1:p.Val1391Ala
ENST00000361418.9:c.4235T>C	ENSP00000354878.5:p.Val1412Ala
ENST00000361961.7:c.4196T>C	ENSP00000354851.3:p.Val1399Ala
ENST00000541463.6:c.4076T>C	ENSP00000438075.2:p.Val1359Ala
ENST00000544797.6:c.4124T>C	ENSP00000445606.2:p.Val1375Ala
ENST00000547733.1:n.1549T>C
ENST00000551264.5:c.1178T>C	ENSP00000448792.1:p.Val393Ala
ENST00000552961.5:c.2137T>C
NM_001173463.1:c.4124T>C	NP_001166934.1:p.Val1375Ala
NM_001173464.1:c.4235T>C	NP_001166935.1:p.Val1412Ala
NM_001173465.1:c.4076T>C	NP_001166936.1:p.Val1359Ala
NM_017641.3:c.4196T>C	NP_060111.2:p.Val1399Ala
XM_005269007.1:c.4238T>C	XP_005269064.1:p.Val1413Ala
XM_005269008.1:c.4223T>C	XP_005269065.1:p.Val1408Ala
XM_005269009.1:c.4217T>C	XP_005269066.1:p.Val1406Ala
XM_005269010.1:c.4199T>C	XP_005269067.1:p.Val1400Ala
XM_005269011.1:c.4184T>C	XP_005269068.1:p.Val1395Ala
XM_005269012.1:c.4109T>C	XP_005269069.1:p.Val1370Ala
XM_005269013.1:c.4094T>C	XP_005269070.1:p.Val1365Ala
XM_005269014.1:c.4055T>C	XP_005269071.1:p.Val1352Ala
XM_006719493.1:c.4178T>C	XP_006719556.1:p.Val1393Ala
XM_006719494.1:c.4106T>C	XP_006719557.1:p.Val1369Ala
XM_006719496.1:c.4163T>C	XP_006719559.1:p.Val1388Ala
XM_011538556.1:c.4169T>C	XP_011536858.1:p.Val1390Ala
XM_005269007.3:c.4238T>C	XP_005269064.1:p.Val1413Ala
XM_005269008.3:c.4223T>C	XP_005269065.1:p.Val1408Ala
XM_005269009.3:c.4217T>C	XP_005269066.1:p.Val1406Ala
XM_005269010.3:c.4199T>C	XP_005269067.1:p.Val1400Ala
XM_005269011.3:c.4184T>C	XP_005269068.1:p.Val1395Ala
XM_005269012.3:c.4109T>C	XP_005269069.1:p.Val1370Ala
XM_005269013.3:c.4094T>C	XP_005269070.1:p.Val1365Ala
XM_005269014.3:c.4055T>C	XP_005269071.1:p.Val1352Ala
XM_006719493.3:c.4178T>C	XP_006719556.1:p.Val1393Ala
XM_006719494.3:c.4106T>C	XP_006719557.1:p.Val1369Ala
XM_011538556.3:c.4169T>C	XP_011536858.1:p.Val1390Ala
XM_017019607.2:c.4184T>C	XP_016875096.1:p.Val1395Ala
XM_017019608.2:c.4145T>C	XP_016875097.1:p.Val1382Ala
XM_017019609.2:c.4034T>C	XP_016875098.1:p.Val1345Ala
XM_017019610.2:c.4034T>C	XP_016875099.1:p.Val1345Ala
XM_017019611.2:c.4016T>C	XP_016875100.1:p.Val1339Ala
NM_001173463.2:c.4124T>C	NP_001166934.1:p.Val1375Ala
NM_001173464.2:c.4235T>C MANE Select	NP_001166935.1:p.Val1412Ala
NM_001173465.2:c.4076T>C	NP_001166936.1:p.Val1359Ala
NM_017641.4:c.4196T>C	NP_060111.2:p.Val1399Ala
NM_001378439.1:c.4238T>C	NP_001365368.1:p.Val1413Ala
NM_001378440.1:c.4223T>C	NP_001365369.1:p.Val1408Ala
NM_001378441.1:c.4199T>C	NP_001365370.1:p.Val1400Ala