Canonical Allele Identifier: CA384387349

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703485T>G (hg19) ; chr12:g.39309683T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309683T>G , CM000674.2:g.39309683T>G	GRCh38
NC_000012.11:g.39703485T>G , CM000674.1:g.39703485T>G	GRCh37
NC_000012.10:g.37989752T>G	NCBI36
NG_017067.1:g.138708A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4180A>C MANE Select	ENSP00000354878.5:p.Lys1394Gln
ENST00000636569.1:c.4117A>C	ENSP00000490369.1:p.Lys1373Gln
ENST00000361418.9:c.4180A>C	ENSP00000354878.5:p.Lys1394Gln
ENST00000361961.7:c.4141A>C	ENSP00000354851.3:p.Lys1381Gln
ENST00000541463.6:c.4021A>C	ENSP00000438075.2:p.Lys1341Gln
ENST00000544797.6:c.4069A>C	ENSP00000445606.2:p.Lys1357Gln
ENST00000547733.1:n.1494A>C
ENST00000551264.5:c.1123A>C	ENSP00000448792.1:p.Lys375Gln
ENST00000552961.5:c.2082A>C
NM_001173463.1:c.4069A>C	NP_001166934.1:p.Lys1357Gln
NM_001173464.1:c.4180A>C	NP_001166935.1:p.Lys1394Gln
NM_001173465.1:c.4021A>C	NP_001166936.1:p.Lys1341Gln
NM_017641.3:c.4141A>C	NP_060111.2:p.Lys1381Gln
XM_005269007.1:c.4183A>C	XP_005269064.1:p.Lys1395Gln
XM_005269008.1:c.4168A>C	XP_005269065.1:p.Lys1390Gln
XM_005269009.1:c.4162A>C	XP_005269066.1:p.Lys1388Gln
XM_005269010.1:c.4144A>C	XP_005269067.1:p.Lys1382Gln
XM_005269011.1:c.4129A>C	XP_005269068.1:p.Lys1377Gln
XM_005269012.1:c.4054A>C	XP_005269069.1:p.Lys1352Gln
XM_005269013.1:c.4039A>C	XP_005269070.1:p.Lys1347Gln
XM_005269014.1:c.4000A>C	XP_005269071.1:p.Lys1334Gln
XM_006719493.1:c.4123A>C	XP_006719556.1:p.Lys1375Gln
XM_006719494.1:c.4051A>C	XP_006719557.1:p.Lys1351Gln
XM_006719496.1:c.4108A>C	XP_006719559.1:p.Lys1370Gln
XM_011538556.1:c.4114A>C	XP_011536858.1:p.Lys1372Gln
XM_005269007.3:c.4183A>C	XP_005269064.1:p.Lys1395Gln
XM_005269008.3:c.4168A>C	XP_005269065.1:p.Lys1390Gln
XM_005269009.3:c.4162A>C	XP_005269066.1:p.Lys1388Gln
XM_005269010.3:c.4144A>C	XP_005269067.1:p.Lys1382Gln
XM_005269011.3:c.4129A>C	XP_005269068.1:p.Lys1377Gln
XM_005269012.3:c.4054A>C	XP_005269069.1:p.Lys1352Gln
XM_005269013.3:c.4039A>C	XP_005269070.1:p.Lys1347Gln
XM_005269014.3:c.4000A>C	XP_005269071.1:p.Lys1334Gln
XM_006719493.3:c.4123A>C	XP_006719556.1:p.Lys1375Gln
XM_006719494.3:c.4051A>C	XP_006719557.1:p.Lys1351Gln
XM_011538556.3:c.4114A>C	XP_011536858.1:p.Lys1372Gln
XM_017019607.2:c.4129A>C	XP_016875096.1:p.Lys1377Gln
XM_017019608.2:c.4090A>C	XP_016875097.1:p.Lys1364Gln
XM_017019609.2:c.3979A>C	XP_016875098.1:p.Lys1327Gln
XM_017019610.2:c.3979A>C	XP_016875099.1:p.Lys1327Gln
XM_017019611.2:c.3961A>C	XP_016875100.1:p.Lys1321Gln
NM_001173463.2:c.4069A>C	NP_001166934.1:p.Lys1357Gln
NM_001173464.2:c.4180A>C MANE Select	NP_001166935.1:p.Lys1394Gln
NM_001173465.2:c.4021A>C	NP_001166936.1:p.Lys1341Gln
NM_017641.4:c.4141A>C	NP_060111.2:p.Lys1381Gln
NM_001378439.1:c.4183A>C	NP_001365368.1:p.Lys1395Gln
NM_001378440.1:c.4168A>C	NP_001365369.1:p.Lys1390Gln
NM_001378441.1:c.4144A>C	NP_001365370.1:p.Lys1382Gln