Canonical Allele Identifier: CA384387376

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703491A>C (hg19) ; chr12:g.39309689A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309689A>C , CM000674.2:g.39309689A>C	GRCh38
NC_000012.11:g.39703491A>C , CM000674.1:g.39703491A>C	GRCh37
NC_000012.10:g.37989758A>C	NCBI36
NG_017067.1:g.138702T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4174T>G MANE Select	ENSP00000354878.5:p.Ser1392Ala
ENST00000636569.1:c.4111T>G	ENSP00000490369.1:p.Ser1371Ala
ENST00000361418.9:c.4174T>G	ENSP00000354878.5:p.Ser1392Ala
ENST00000361961.7:c.4135T>G	ENSP00000354851.3:p.Ser1379Ala
ENST00000541463.6:c.4015T>G	ENSP00000438075.2:p.Ser1339Ala
ENST00000544797.6:c.4063T>G	ENSP00000445606.2:p.Ser1355Ala
ENST00000547733.1:n.1488T>G
ENST00000551264.5:c.1117T>G	ENSP00000448792.1:p.Ser373Ala
ENST00000552961.5:c.2076T>G
NM_001173463.1:c.4063T>G	NP_001166934.1:p.Ser1355Ala
NM_001173464.1:c.4174T>G	NP_001166935.1:p.Ser1392Ala
NM_001173465.1:c.4015T>G	NP_001166936.1:p.Ser1339Ala
NM_017641.3:c.4135T>G	NP_060111.2:p.Ser1379Ala
XM_005269007.1:c.4177T>G	XP_005269064.1:p.Ser1393Ala
XM_005269008.1:c.4162T>G	XP_005269065.1:p.Ser1388Ala
XM_005269009.1:c.4156T>G	XP_005269066.1:p.Ser1386Ala
XM_005269010.1:c.4138T>G	XP_005269067.1:p.Ser1380Ala
XM_005269011.1:c.4123T>G	XP_005269068.1:p.Ser1375Ala
XM_005269012.1:c.4048T>G	XP_005269069.1:p.Ser1350Ala
XM_005269013.1:c.4033T>G	XP_005269070.1:p.Ser1345Ala
XM_005269014.1:c.3994T>G	XP_005269071.1:p.Ser1332Ala
XM_006719493.1:c.4117T>G	XP_006719556.1:p.Ser1373Ala
XM_006719494.1:c.4045T>G	XP_006719557.1:p.Ser1349Ala
XM_006719496.1:c.4102T>G	XP_006719559.1:p.Ser1368Ala
XM_011538556.1:c.4108T>G	XP_011536858.1:p.Ser1370Ala
XM_005269007.3:c.4177T>G	XP_005269064.1:p.Ser1393Ala
XM_005269008.3:c.4162T>G	XP_005269065.1:p.Ser1388Ala
XM_005269009.3:c.4156T>G	XP_005269066.1:p.Ser1386Ala
XM_005269010.3:c.4138T>G	XP_005269067.1:p.Ser1380Ala
XM_005269011.3:c.4123T>G	XP_005269068.1:p.Ser1375Ala
XM_005269012.3:c.4048T>G	XP_005269069.1:p.Ser1350Ala
XM_005269013.3:c.4033T>G	XP_005269070.1:p.Ser1345Ala
XM_005269014.3:c.3994T>G	XP_005269071.1:p.Ser1332Ala
XM_006719493.3:c.4117T>G	XP_006719556.1:p.Ser1373Ala
XM_006719494.3:c.4045T>G	XP_006719557.1:p.Ser1349Ala
XM_011538556.3:c.4108T>G	XP_011536858.1:p.Ser1370Ala
XM_017019607.2:c.4123T>G	XP_016875096.1:p.Ser1375Ala
XM_017019608.2:c.4084T>G	XP_016875097.1:p.Ser1362Ala
XM_017019609.2:c.3973T>G	XP_016875098.1:p.Ser1325Ala
XM_017019610.2:c.3973T>G	XP_016875099.1:p.Ser1325Ala
XM_017019611.2:c.3955T>G	XP_016875100.1:p.Ser1319Ala
NM_001173463.2:c.4063T>G	NP_001166934.1:p.Ser1355Ala
NM_001173464.2:c.4174T>G MANE Select	NP_001166935.1:p.Ser1392Ala
NM_001173465.2:c.4015T>G	NP_001166936.1:p.Ser1339Ala
NM_017641.4:c.4135T>G	NP_060111.2:p.Ser1379Ala
NM_001378439.1:c.4177T>G	NP_001365368.1:p.Ser1393Ala
NM_001378440.1:c.4162T>G	NP_001365369.1:p.Ser1388Ala
NM_001378441.1:c.4138T>G	NP_001365370.1:p.Ser1380Ala