Canonical Allele Identifier: CA384386969

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703427C>T (hg19) ; chr12:g.39309625C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309625C>T , CM000674.2:g.39309625C>T	GRCh38
NC_000012.11:g.39703427C>T , CM000674.1:g.39703427C>T	GRCh37
NC_000012.10:g.37989694C>T	NCBI36
NG_017067.1:g.138766G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4238G>A MANE Select	ENSP00000354878.5:p.Trp1413Ter
ENST00000636569.1:c.4175G>A	ENSP00000490369.1:p.Trp1392Ter
ENST00000361418.9:c.4238G>A	ENSP00000354878.5:p.Trp1413Ter
ENST00000361961.7:c.4199G>A	ENSP00000354851.3:p.Trp1400Ter
ENST00000541463.6:c.4079G>A	ENSP00000438075.2:p.Trp1360Ter
ENST00000544797.6:c.4127G>A	ENSP00000445606.2:p.Trp1376Ter
ENST00000547733.1:n.1552G>A
ENST00000551264.5:c.1181G>A	ENSP00000448792.1:p.Trp394Ter
ENST00000552961.5:c.2140G>A
NM_001173463.1:c.4127G>A	NP_001166934.1:p.Trp1376Ter
NM_001173464.1:c.4238G>A	NP_001166935.1:p.Trp1413Ter
NM_001173465.1:c.4079G>A	NP_001166936.1:p.Trp1360Ter
NM_017641.3:c.4199G>A	NP_060111.2:p.Trp1400Ter
XM_005269007.1:c.4241G>A	XP_005269064.1:p.Trp1414Ter
XM_005269008.1:c.4226G>A	XP_005269065.1:p.Trp1409Ter
XM_005269009.1:c.4220G>A	XP_005269066.1:p.Trp1407Ter
XM_005269010.1:c.4202G>A	XP_005269067.1:p.Trp1401Ter
XM_005269011.1:c.4187G>A	XP_005269068.1:p.Trp1396Ter
XM_005269012.1:c.4112G>A	XP_005269069.1:p.Trp1371Ter
XM_005269013.1:c.4097G>A	XP_005269070.1:p.Trp1366Ter
XM_005269014.1:c.4058G>A	XP_005269071.1:p.Trp1353Ter
XM_006719493.1:c.4181G>A	XP_006719556.1:p.Trp1394Ter
XM_006719494.1:c.4109G>A	XP_006719557.1:p.Trp1370Ter
XM_006719496.1:c.4166G>A	XP_006719559.1:p.Trp1389Ter
XM_011538556.1:c.4172G>A	XP_011536858.1:p.Trp1391Ter
XM_005269007.3:c.4241G>A	XP_005269064.1:p.Trp1414Ter
XM_005269008.3:c.4226G>A	XP_005269065.1:p.Trp1409Ter
XM_005269009.3:c.4220G>A	XP_005269066.1:p.Trp1407Ter
XM_005269010.3:c.4202G>A	XP_005269067.1:p.Trp1401Ter
XM_005269011.3:c.4187G>A	XP_005269068.1:p.Trp1396Ter
XM_005269012.3:c.4112G>A	XP_005269069.1:p.Trp1371Ter
XM_005269013.3:c.4097G>A	XP_005269070.1:p.Trp1366Ter
XM_005269014.3:c.4058G>A	XP_005269071.1:p.Trp1353Ter
XM_006719493.3:c.4181G>A	XP_006719556.1:p.Trp1394Ter
XM_006719494.3:c.4109G>A	XP_006719557.1:p.Trp1370Ter
XM_011538556.3:c.4172G>A	XP_011536858.1:p.Trp1391Ter
XM_017019607.2:c.4187G>A	XP_016875096.1:p.Trp1396Ter
XM_017019608.2:c.4148G>A	XP_016875097.1:p.Trp1383Ter
XM_017019609.2:c.4037G>A	XP_016875098.1:p.Trp1346Ter
XM_017019610.2:c.4037G>A	XP_016875099.1:p.Trp1346Ter
XM_017019611.2:c.4019G>A	XP_016875100.1:p.Trp1340Ter
NM_001173463.2:c.4127G>A	NP_001166934.1:p.Trp1376Ter
NM_001173464.2:c.4238G>A MANE Select	NP_001166935.1:p.Trp1413Ter
NM_001173465.2:c.4079G>A	NP_001166936.1:p.Trp1360Ter
NM_017641.4:c.4199G>A	NP_060111.2:p.Trp1400Ter
NM_001378439.1:c.4241G>A	NP_001365368.1:p.Trp1414Ter
NM_001378440.1:c.4226G>A	NP_001365369.1:p.Trp1409Ter
NM_001378441.1:c.4202G>A	NP_001365370.1:p.Trp1401Ter