Canonical Allele Identifier: CA384387373

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703490G>T (hg19) ; chr12:g.39309688G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309688G>T , CM000674.2:g.39309688G>T	GRCh38
NC_000012.11:g.39703490G>T , CM000674.1:g.39703490G>T	GRCh37
NC_000012.10:g.37989757G>T	NCBI36
NG_017067.1:g.138703C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4175C>A MANE Select	ENSP00000354878.5:p.Ser1392Tyr
ENST00000636569.1:c.4112C>A	ENSP00000490369.1:p.Ser1371Tyr
ENST00000361418.9:c.4175C>A	ENSP00000354878.5:p.Ser1392Tyr
ENST00000361961.7:c.4136C>A	ENSP00000354851.3:p.Ser1379Tyr
ENST00000541463.6:c.4016C>A	ENSP00000438075.2:p.Ser1339Tyr
ENST00000544797.6:c.4064C>A	ENSP00000445606.2:p.Ser1355Tyr
ENST00000547733.1:n.1489C>A
ENST00000551264.5:c.1118C>A	ENSP00000448792.1:p.Ser373Tyr
ENST00000552961.5:c.2077C>A
NM_001173463.1:c.4064C>A	NP_001166934.1:p.Ser1355Tyr
NM_001173464.1:c.4175C>A	NP_001166935.1:p.Ser1392Tyr
NM_001173465.1:c.4016C>A	NP_001166936.1:p.Ser1339Tyr
NM_017641.3:c.4136C>A	NP_060111.2:p.Ser1379Tyr
XM_005269007.1:c.4178C>A	XP_005269064.1:p.Ser1393Tyr
XM_005269008.1:c.4163C>A	XP_005269065.1:p.Ser1388Tyr
XM_005269009.1:c.4157C>A	XP_005269066.1:p.Ser1386Tyr
XM_005269010.1:c.4139C>A	XP_005269067.1:p.Ser1380Tyr
XM_005269011.1:c.4124C>A	XP_005269068.1:p.Ser1375Tyr
XM_005269012.1:c.4049C>A	XP_005269069.1:p.Ser1350Tyr
XM_005269013.1:c.4034C>A	XP_005269070.1:p.Ser1345Tyr
XM_005269014.1:c.3995C>A	XP_005269071.1:p.Ser1332Tyr
XM_006719493.1:c.4118C>A	XP_006719556.1:p.Ser1373Tyr
XM_006719494.1:c.4046C>A	XP_006719557.1:p.Ser1349Tyr
XM_006719496.1:c.4103C>A	XP_006719559.1:p.Ser1368Tyr
XM_011538556.1:c.4109C>A	XP_011536858.1:p.Ser1370Tyr
XM_005269007.3:c.4178C>A	XP_005269064.1:p.Ser1393Tyr
XM_005269008.3:c.4163C>A	XP_005269065.1:p.Ser1388Tyr
XM_005269009.3:c.4157C>A	XP_005269066.1:p.Ser1386Tyr
XM_005269010.3:c.4139C>A	XP_005269067.1:p.Ser1380Tyr
XM_005269011.3:c.4124C>A	XP_005269068.1:p.Ser1375Tyr
XM_005269012.3:c.4049C>A	XP_005269069.1:p.Ser1350Tyr
XM_005269013.3:c.4034C>A	XP_005269070.1:p.Ser1345Tyr
XM_005269014.3:c.3995C>A	XP_005269071.1:p.Ser1332Tyr
XM_006719493.3:c.4118C>A	XP_006719556.1:p.Ser1373Tyr
XM_006719494.3:c.4046C>A	XP_006719557.1:p.Ser1349Tyr
XM_011538556.3:c.4109C>A	XP_011536858.1:p.Ser1370Tyr
XM_017019607.2:c.4124C>A	XP_016875096.1:p.Ser1375Tyr
XM_017019608.2:c.4085C>A	XP_016875097.1:p.Ser1362Tyr
XM_017019609.2:c.3974C>A	XP_016875098.1:p.Ser1325Tyr
XM_017019610.2:c.3974C>A	XP_016875099.1:p.Ser1325Tyr
XM_017019611.2:c.3956C>A	XP_016875100.1:p.Ser1319Tyr
NM_001173463.2:c.4064C>A	NP_001166934.1:p.Ser1355Tyr
NM_001173464.2:c.4175C>A MANE Select	NP_001166935.1:p.Ser1392Tyr
NM_001173465.2:c.4016C>A	NP_001166936.1:p.Ser1339Tyr
NM_017641.4:c.4136C>A	NP_060111.2:p.Ser1379Tyr
NM_001378439.1:c.4178C>A	NP_001365368.1:p.Ser1393Tyr
NM_001378440.1:c.4163C>A	NP_001365369.1:p.Ser1388Tyr
NM_001378441.1:c.4139C>A	NP_001365370.1:p.Ser1380Tyr