Canonical Allele Identifier: CA384387133

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703455T>G (hg19) ; chr12:g.39309653T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309653T>G , CM000674.2:g.39309653T>G	GRCh38
NC_000012.11:g.39703455T>G , CM000674.1:g.39703455T>G	GRCh37
NC_000012.10:g.37989722T>G	NCBI36
NG_017067.1:g.138738A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4210A>C MANE Select	ENSP00000354878.5:p.Thr1404Pro
ENST00000636569.1:c.4147A>C	ENSP00000490369.1:p.Thr1383Pro
ENST00000361418.9:c.4210A>C	ENSP00000354878.5:p.Thr1404Pro
ENST00000361961.7:c.4171A>C	ENSP00000354851.3:p.Thr1391Pro
ENST00000541463.6:c.4051A>C	ENSP00000438075.2:p.Thr1351Pro
ENST00000544797.6:c.4099A>C	ENSP00000445606.2:p.Thr1367Pro
ENST00000547733.1:n.1524A>C
ENST00000551264.5:c.1153A>C	ENSP00000448792.1:p.Thr385Pro
ENST00000552961.5:c.2112A>C
NM_001173463.1:c.4099A>C	NP_001166934.1:p.Thr1367Pro
NM_001173464.1:c.4210A>C	NP_001166935.1:p.Thr1404Pro
NM_001173465.1:c.4051A>C	NP_001166936.1:p.Thr1351Pro
NM_017641.3:c.4171A>C	NP_060111.2:p.Thr1391Pro
XM_005269007.1:c.4213A>C	XP_005269064.1:p.Thr1405Pro
XM_005269008.1:c.4198A>C	XP_005269065.1:p.Thr1400Pro
XM_005269009.1:c.4192A>C	XP_005269066.1:p.Thr1398Pro
XM_005269010.1:c.4174A>C	XP_005269067.1:p.Thr1392Pro
XM_005269011.1:c.4159A>C	XP_005269068.1:p.Thr1387Pro
XM_005269012.1:c.4084A>C	XP_005269069.1:p.Thr1362Pro
XM_005269013.1:c.4069A>C	XP_005269070.1:p.Thr1357Pro
XM_005269014.1:c.4030A>C	XP_005269071.1:p.Thr1344Pro
XM_006719493.1:c.4153A>C	XP_006719556.1:p.Thr1385Pro
XM_006719494.1:c.4081A>C	XP_006719557.1:p.Thr1361Pro
XM_006719496.1:c.4138A>C	XP_006719559.1:p.Thr1380Pro
XM_011538556.1:c.4144A>C	XP_011536858.1:p.Thr1382Pro
XM_005269007.3:c.4213A>C	XP_005269064.1:p.Thr1405Pro
XM_005269008.3:c.4198A>C	XP_005269065.1:p.Thr1400Pro
XM_005269009.3:c.4192A>C	XP_005269066.1:p.Thr1398Pro
XM_005269010.3:c.4174A>C	XP_005269067.1:p.Thr1392Pro
XM_005269011.3:c.4159A>C	XP_005269068.1:p.Thr1387Pro
XM_005269012.3:c.4084A>C	XP_005269069.1:p.Thr1362Pro
XM_005269013.3:c.4069A>C	XP_005269070.1:p.Thr1357Pro
XM_005269014.3:c.4030A>C	XP_005269071.1:p.Thr1344Pro
XM_006719493.3:c.4153A>C	XP_006719556.1:p.Thr1385Pro
XM_006719494.3:c.4081A>C	XP_006719557.1:p.Thr1361Pro
XM_011538556.3:c.4144A>C	XP_011536858.1:p.Thr1382Pro
XM_017019607.2:c.4159A>C	XP_016875096.1:p.Thr1387Pro
XM_017019608.2:c.4120A>C	XP_016875097.1:p.Thr1374Pro
XM_017019609.2:c.4009A>C	XP_016875098.1:p.Thr1337Pro
XM_017019610.2:c.4009A>C	XP_016875099.1:p.Thr1337Pro
XM_017019611.2:c.3991A>C	XP_016875100.1:p.Thr1331Pro
NM_001173463.2:c.4099A>C	NP_001166934.1:p.Thr1367Pro
NM_001173464.2:c.4210A>C MANE Select	NP_001166935.1:p.Thr1404Pro
NM_001173465.2:c.4051A>C	NP_001166936.1:p.Thr1351Pro
NM_017641.4:c.4171A>C	NP_060111.2:p.Thr1391Pro
NM_001378439.1:c.4213A>C	NP_001365368.1:p.Thr1405Pro
NM_001378440.1:c.4198A>C	NP_001365369.1:p.Thr1400Pro
NM_001378441.1:c.4174A>C	NP_001365370.1:p.Thr1392Pro