Canonical Allele Identifier: CA6510235

Gene: KIF21A

Linked Data

• dbSNP Id: rs758321044
• ExAC: 12:39703458 A / G
• gnomAD v2: 12-39703458-A-G
• MyVariant Identifiers: chr12:g.39703458A>G (hg19) ; chr12:g.39309656A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309656A>G , CM000674.2:g.39309656A>G	GRCh38
NC_000012.11:g.39703458A>G , CM000674.1:g.39703458A>G	GRCh37
NC_000012.10:g.37989725A>G	NCBI36
NG_017067.1:g.138735T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4207T>C MANE Select	ENSP00000354878.5:p.Phe1403Leu
ENST00000636569.1:c.4144T>C	ENSP00000490369.1:p.Phe1382Leu
ENST00000361418.9:c.4207T>C	ENSP00000354878.5:p.Phe1403Leu
ENST00000361961.7:c.4168T>C	ENSP00000354851.3:p.Phe1390Leu
ENST00000541463.6:c.4048T>C	ENSP00000438075.2:p.Phe1350Leu
ENST00000544797.6:c.4096T>C	ENSP00000445606.2:p.Phe1366Leu
ENST00000547733.1:n.1521T>C
ENST00000551264.5:c.1150T>C	ENSP00000448792.1:p.Phe384Leu
ENST00000552961.5:c.2109T>C
NM_001173463.1:c.4096T>C	NP_001166934.1:p.Phe1366Leu
NM_001173464.1:c.4207T>C	NP_001166935.1:p.Phe1403Leu
NM_001173465.1:c.4048T>C	NP_001166936.1:p.Phe1350Leu
NM_017641.3:c.4168T>C	NP_060111.2:p.Phe1390Leu
XM_005269007.1:c.4210T>C	XP_005269064.1:p.Phe1404Leu
XM_005269008.1:c.4195T>C	XP_005269065.1:p.Phe1399Leu
XM_005269009.1:c.4189T>C	XP_005269066.1:p.Phe1397Leu
XM_005269010.1:c.4171T>C	XP_005269067.1:p.Phe1391Leu
XM_005269011.1:c.4156T>C	XP_005269068.1:p.Phe1386Leu
XM_005269012.1:c.4081T>C	XP_005269069.1:p.Phe1361Leu
XM_005269013.1:c.4066T>C	XP_005269070.1:p.Phe1356Leu
XM_005269014.1:c.4027T>C	XP_005269071.1:p.Phe1343Leu
XM_006719493.1:c.4150T>C	XP_006719556.1:p.Phe1384Leu
XM_006719494.1:c.4078T>C	XP_006719557.1:p.Phe1360Leu
XM_006719496.1:c.4135T>C	XP_006719559.1:p.Phe1379Leu
XM_011538556.1:c.4141T>C	XP_011536858.1:p.Phe1381Leu
XM_005269007.3:c.4210T>C	XP_005269064.1:p.Phe1404Leu
XM_005269008.3:c.4195T>C	XP_005269065.1:p.Phe1399Leu
XM_005269009.3:c.4189T>C	XP_005269066.1:p.Phe1397Leu
XM_005269010.3:c.4171T>C	XP_005269067.1:p.Phe1391Leu
XM_005269011.3:c.4156T>C	XP_005269068.1:p.Phe1386Leu
XM_005269012.3:c.4081T>C	XP_005269069.1:p.Phe1361Leu
XM_005269013.3:c.4066T>C	XP_005269070.1:p.Phe1356Leu
XM_005269014.3:c.4027T>C	XP_005269071.1:p.Phe1343Leu
XM_006719493.3:c.4150T>C	XP_006719556.1:p.Phe1384Leu
XM_006719494.3:c.4078T>C	XP_006719557.1:p.Phe1360Leu
XM_011538556.3:c.4141T>C	XP_011536858.1:p.Phe1381Leu
XM_017019607.2:c.4156T>C	XP_016875096.1:p.Phe1386Leu
XM_017019608.2:c.4117T>C	XP_016875097.1:p.Phe1373Leu
XM_017019609.2:c.4006T>C	XP_016875098.1:p.Phe1336Leu
XM_017019610.2:c.4006T>C	XP_016875099.1:p.Phe1336Leu
XM_017019611.2:c.3988T>C	XP_016875100.1:p.Phe1330Leu
NM_001173463.2:c.4096T>C	NP_001166934.1:p.Phe1366Leu
NM_001173464.2:c.4207T>C MANE Select	NP_001166935.1:p.Phe1403Leu
NM_001173465.2:c.4048T>C	NP_001166936.1:p.Phe1350Leu
NM_017641.4:c.4168T>C	NP_060111.2:p.Phe1390Leu
NM_001378439.1:c.4210T>C	NP_001365368.1:p.Phe1404Leu
NM_001378440.1:c.4195T>C	NP_001365369.1:p.Phe1399Leu
NM_001378441.1:c.4171T>C	NP_001365370.1:p.Phe1391Leu