Canonical Allele Identifier: CA384387343

Gene: KIF21A

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4180A>T MANE Select	ENSP00000354878.5:p.Lys1394Ter
ENST00000636569.1:c.4117A>T	ENSP00000490369.1:p.Lys1373Ter
ENST00000361418.9:c.4180A>T	ENSP00000354878.5:p.Lys1394Ter
ENST00000361961.7:c.4141A>T	ENSP00000354851.3:p.Lys1381Ter
ENST00000541463.6:c.4021A>T	ENSP00000438075.2:p.Lys1341Ter
ENST00000544797.6:c.4069A>T	ENSP00000445606.2:p.Lys1357Ter
ENST00000547733.1:n.1494A>T
ENST00000551264.5:c.1123A>T	ENSP00000448792.1:p.Lys375Ter
ENST00000552961.5:c.2082A>T
NM_001173463.1:c.4069A>T	NP_001166934.1:p.Lys1357Ter
NM_001173464.1:c.4180A>T	NP_001166935.1:p.Lys1394Ter
NM_001173465.1:c.4021A>T	NP_001166936.1:p.Lys1341Ter
NM_017641.3:c.4141A>T	NP_060111.2:p.Lys1381Ter
XM_005269007.1:c.4183A>T	XP_005269064.1:p.Lys1395Ter
XM_005269008.1:c.4168A>T	XP_005269065.1:p.Lys1390Ter
XM_005269009.1:c.4162A>T	XP_005269066.1:p.Lys1388Ter
XM_005269010.1:c.4144A>T	XP_005269067.1:p.Lys1382Ter
XM_005269011.1:c.4129A>T	XP_005269068.1:p.Lys1377Ter
XM_005269012.1:c.4054A>T	XP_005269069.1:p.Lys1352Ter
XM_005269013.1:c.4039A>T	XP_005269070.1:p.Lys1347Ter
XM_005269014.1:c.4000A>T	XP_005269071.1:p.Lys1334Ter
XM_006719493.1:c.4123A>T	XP_006719556.1:p.Lys1375Ter
XM_006719494.1:c.4051A>T	XP_006719557.1:p.Lys1351Ter
XM_006719496.1:c.4108A>T	XP_006719559.1:p.Lys1370Ter
XM_011538556.1:c.4114A>T	XP_011536858.1:p.Lys1372Ter
XM_005269007.3:c.4183A>T	XP_005269064.1:p.Lys1395Ter
XM_005269008.3:c.4168A>T	XP_005269065.1:p.Lys1390Ter
XM_005269009.3:c.4162A>T	XP_005269066.1:p.Lys1388Ter
XM_005269010.3:c.4144A>T	XP_005269067.1:p.Lys1382Ter
XM_005269011.3:c.4129A>T	XP_005269068.1:p.Lys1377Ter
XM_005269012.3:c.4054A>T	XP_005269069.1:p.Lys1352Ter
XM_005269013.3:c.4039A>T	XP_005269070.1:p.Lys1347Ter
XM_005269014.3:c.4000A>T	XP_005269071.1:p.Lys1334Ter
XM_006719493.3:c.4123A>T	XP_006719556.1:p.Lys1375Ter
XM_006719494.3:c.4051A>T	XP_006719557.1:p.Lys1351Ter
XM_011538556.3:c.4114A>T	XP_011536858.1:p.Lys1372Ter
XM_017019607.2:c.4129A>T	XP_016875096.1:p.Lys1377Ter
XM_017019608.2:c.4090A>T	XP_016875097.1:p.Lys1364Ter
XM_017019609.2:c.3979A>T	XP_016875098.1:p.Lys1327Ter
XM_017019610.2:c.3979A>T	XP_016875099.1:p.Lys1327Ter
XM_017019611.2:c.3961A>T	XP_016875100.1:p.Lys1321Ter
NM_001173463.2:c.4069A>T	NP_001166934.1:p.Lys1357Ter
NM_001173464.2:c.4180A>T MANE Select	NP_001166935.1:p.Lys1394Ter
NM_001173465.2:c.4021A>T	NP_001166936.1:p.Lys1341Ter
NM_017641.4:c.4141A>T	NP_060111.2:p.Lys1381Ter
NM_001378439.1:c.4183A>T	NP_001365368.1:p.Lys1395Ter
NM_001378440.1:c.4168A>T	NP_001365369.1:p.Lys1390Ter
NM_001378441.1:c.4144A>T	NP_001365370.1:p.Lys1382Ter