Canonical Allele Identifier: CA384387330

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703482A>G (hg19) ; chr12:g.39309680A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309680A>G , CM000674.2:g.39309680A>G	GRCh38
NC_000012.11:g.39703482A>G , CM000674.1:g.39703482A>G	GRCh37
NC_000012.10:g.37989749A>G	NCBI36
NG_017067.1:g.138711T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4183T>C MANE Select	ENSP00000354878.5:p.Tyr1395His
ENST00000636569.1:c.4120T>C	ENSP00000490369.1:p.Tyr1374His
ENST00000361418.9:c.4183T>C	ENSP00000354878.5:p.Tyr1395His
ENST00000361961.7:c.4144T>C	ENSP00000354851.3:p.Tyr1382His
ENST00000541463.6:c.4024T>C	ENSP00000438075.2:p.Tyr1342His
ENST00000544797.6:c.4072T>C	ENSP00000445606.2:p.Tyr1358His
ENST00000547733.1:n.1497T>C
ENST00000551264.5:c.1126T>C	ENSP00000448792.1:p.Tyr376His
ENST00000552961.5:c.2085T>C
NM_001173463.1:c.4072T>C	NP_001166934.1:p.Tyr1358His
NM_001173464.1:c.4183T>C	NP_001166935.1:p.Tyr1395His
NM_001173465.1:c.4024T>C	NP_001166936.1:p.Tyr1342His
NM_017641.3:c.4144T>C	NP_060111.2:p.Tyr1382His
XM_005269007.1:c.4186T>C	XP_005269064.1:p.Tyr1396His
XM_005269008.1:c.4171T>C	XP_005269065.1:p.Tyr1391His
XM_005269009.1:c.4165T>C	XP_005269066.1:p.Tyr1389His
XM_005269010.1:c.4147T>C	XP_005269067.1:p.Tyr1383His
XM_005269011.1:c.4132T>C	XP_005269068.1:p.Tyr1378His
XM_005269012.1:c.4057T>C	XP_005269069.1:p.Tyr1353His
XM_005269013.1:c.4042T>C	XP_005269070.1:p.Tyr1348His
XM_005269014.1:c.4003T>C	XP_005269071.1:p.Tyr1335His
XM_006719493.1:c.4126T>C	XP_006719556.1:p.Tyr1376His
XM_006719494.1:c.4054T>C	XP_006719557.1:p.Tyr1352His
XM_006719496.1:c.4111T>C	XP_006719559.1:p.Tyr1371His
XM_011538556.1:c.4117T>C	XP_011536858.1:p.Tyr1373His
XM_005269007.3:c.4186T>C	XP_005269064.1:p.Tyr1396His
XM_005269008.3:c.4171T>C	XP_005269065.1:p.Tyr1391His
XM_005269009.3:c.4165T>C	XP_005269066.1:p.Tyr1389His
XM_005269010.3:c.4147T>C	XP_005269067.1:p.Tyr1383His
XM_005269011.3:c.4132T>C	XP_005269068.1:p.Tyr1378His
XM_005269012.3:c.4057T>C	XP_005269069.1:p.Tyr1353His
XM_005269013.3:c.4042T>C	XP_005269070.1:p.Tyr1348His
XM_005269014.3:c.4003T>C	XP_005269071.1:p.Tyr1335His
XM_006719493.3:c.4126T>C	XP_006719556.1:p.Tyr1376His
XM_006719494.3:c.4054T>C	XP_006719557.1:p.Tyr1352His
XM_011538556.3:c.4117T>C	XP_011536858.1:p.Tyr1373His
XM_017019607.2:c.4132T>C	XP_016875096.1:p.Tyr1378His
XM_017019608.2:c.4093T>C	XP_016875097.1:p.Tyr1365His
XM_017019609.2:c.3982T>C	XP_016875098.1:p.Tyr1328His
XM_017019610.2:c.3982T>C	XP_016875099.1:p.Tyr1328His
XM_017019611.2:c.3964T>C	XP_016875100.1:p.Tyr1322His
NM_001173463.2:c.4072T>C	NP_001166934.1:p.Tyr1358His
NM_001173464.2:c.4183T>C MANE Select	NP_001166935.1:p.Tyr1395His
NM_001173465.2:c.4024T>C	NP_001166936.1:p.Tyr1342His
NM_017641.4:c.4144T>C	NP_060111.2:p.Tyr1382His
NM_001378439.1:c.4186T>C	NP_001365368.1:p.Tyr1396His
NM_001378440.1:c.4171T>C	NP_001365369.1:p.Tyr1391His
NM_001378441.1:c.4147T>C	NP_001365370.1:p.Tyr1383His