Canonical Allele Identifier: CA384386823

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703406T>G (hg19) ; chr12:g.39309604T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309604T>G , CM000674.2:g.39309604T>G	GRCh38
NC_000012.11:g.39703406T>G , CM000674.1:g.39703406T>G	GRCh37
NC_000012.10:g.37989673T>G	NCBI36
NG_017067.1:g.138787A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4259A>C MANE Select	ENSP00000354878.5:p.Lys1420Thr
ENST00000636569.1:c.4196A>C	ENSP00000490369.1:p.Lys1399Thr
ENST00000361418.9:c.4259A>C	ENSP00000354878.5:p.Lys1420Thr
ENST00000361961.7:c.4220A>C	ENSP00000354851.3:p.Lys1407Thr
ENST00000541463.6:c.4100A>C	ENSP00000438075.2:p.Lys1367Thr
ENST00000544797.6:c.4148A>C	ENSP00000445606.2:p.Lys1383Thr
ENST00000547733.1:n.1573A>C
ENST00000551264.5:c.1202A>C	ENSP00000448792.1:p.Lys401Thr
ENST00000552961.5:c.2161A>C
NM_001173463.1:c.4148A>C	NP_001166934.1:p.Lys1383Thr
NM_001173464.1:c.4259A>C	NP_001166935.1:p.Lys1420Thr
NM_001173465.1:c.4100A>C	NP_001166936.1:p.Lys1367Thr
NM_017641.3:c.4220A>C	NP_060111.2:p.Lys1407Thr
XM_005269007.1:c.4262A>C	XP_005269064.1:p.Lys1421Thr
XM_005269008.1:c.4247A>C	XP_005269065.1:p.Lys1416Thr
XM_005269009.1:c.4241A>C	XP_005269066.1:p.Lys1414Thr
XM_005269010.1:c.4223A>C	XP_005269067.1:p.Lys1408Thr
XM_005269011.1:c.4208A>C	XP_005269068.1:p.Lys1403Thr
XM_005269012.1:c.4133A>C	XP_005269069.1:p.Lys1378Thr
XM_005269013.1:c.4118A>C	XP_005269070.1:p.Lys1373Thr
XM_005269014.1:c.4079A>C	XP_005269071.1:p.Lys1360Thr
XM_006719493.1:c.4202A>C	XP_006719556.1:p.Lys1401Thr
XM_006719494.1:c.4130A>C	XP_006719557.1:p.Lys1377Thr
XM_006719496.1:c.4187A>C	XP_006719559.1:p.Lys1396Thr
XM_011538556.1:c.4193A>C	XP_011536858.1:p.Lys1398Thr
XM_005269007.3:c.4262A>C	XP_005269064.1:p.Lys1421Thr
XM_005269008.3:c.4247A>C	XP_005269065.1:p.Lys1416Thr
XM_005269009.3:c.4241A>C	XP_005269066.1:p.Lys1414Thr
XM_005269010.3:c.4223A>C	XP_005269067.1:p.Lys1408Thr
XM_005269011.3:c.4208A>C	XP_005269068.1:p.Lys1403Thr
XM_005269012.3:c.4133A>C	XP_005269069.1:p.Lys1378Thr
XM_005269013.3:c.4118A>C	XP_005269070.1:p.Lys1373Thr
XM_005269014.3:c.4079A>C	XP_005269071.1:p.Lys1360Thr
XM_006719493.3:c.4202A>C	XP_006719556.1:p.Lys1401Thr
XM_006719494.3:c.4130A>C	XP_006719557.1:p.Lys1377Thr
XM_011538556.3:c.4193A>C	XP_011536858.1:p.Lys1398Thr
XM_017019607.2:c.4208A>C	XP_016875096.1:p.Lys1403Thr
XM_017019608.2:c.4169A>C	XP_016875097.1:p.Lys1390Thr
XM_017019609.2:c.4058A>C	XP_016875098.1:p.Lys1353Thr
XM_017019610.2:c.4058A>C	XP_016875099.1:p.Lys1353Thr
XM_017019611.2:c.4040A>C	XP_016875100.1:p.Lys1347Thr
NM_001173463.2:c.4148A>C	NP_001166934.1:p.Lys1383Thr
NM_001173464.2:c.4259A>C MANE Select	NP_001166935.1:p.Lys1420Thr
NM_001173465.2:c.4100A>C	NP_001166936.1:p.Lys1367Thr
NM_017641.4:c.4220A>C	NP_060111.2:p.Lys1407Thr
NM_001378439.1:c.4262A>C	NP_001365368.1:p.Lys1421Thr
NM_001378440.1:c.4247A>C	NP_001365369.1:p.Lys1416Thr
NM_001378441.1:c.4223A>C	NP_001365370.1:p.Lys1408Thr