Canonical Allele Identifier: CA384387169

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703460A>C (hg19) ; chr12:g.39309658A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309658A>C , CM000674.2:g.39309658A>C	GRCh38
NC_000012.11:g.39703460A>C , CM000674.1:g.39703460A>C	GRCh37
NC_000012.10:g.37989727A>C	NCBI36
NG_017067.1:g.138733T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4205T>G MANE Select	ENSP00000354878.5:p.Val1402Gly
ENST00000636569.1:c.4142T>G	ENSP00000490369.1:p.Val1381Gly
ENST00000361418.9:c.4205T>G	ENSP00000354878.5:p.Val1402Gly
ENST00000361961.7:c.4166T>G	ENSP00000354851.3:p.Val1389Gly
ENST00000541463.6:c.4046T>G	ENSP00000438075.2:p.Val1349Gly
ENST00000544797.6:c.4094T>G	ENSP00000445606.2:p.Val1365Gly
ENST00000547733.1:n.1519T>G
ENST00000551264.5:c.1148T>G	ENSP00000448792.1:p.Val383Gly
ENST00000552961.5:c.2107T>G
NM_001173463.1:c.4094T>G	NP_001166934.1:p.Val1365Gly
NM_001173464.1:c.4205T>G	NP_001166935.1:p.Val1402Gly
NM_001173465.1:c.4046T>G	NP_001166936.1:p.Val1349Gly
NM_017641.3:c.4166T>G	NP_060111.2:p.Val1389Gly
XM_005269007.1:c.4208T>G	XP_005269064.1:p.Val1403Gly
XM_005269008.1:c.4193T>G	XP_005269065.1:p.Val1398Gly
XM_005269009.1:c.4187T>G	XP_005269066.1:p.Val1396Gly
XM_005269010.1:c.4169T>G	XP_005269067.1:p.Val1390Gly
XM_005269011.1:c.4154T>G	XP_005269068.1:p.Val1385Gly
XM_005269012.1:c.4079T>G	XP_005269069.1:p.Val1360Gly
XM_005269013.1:c.4064T>G	XP_005269070.1:p.Val1355Gly
XM_005269014.1:c.4025T>G	XP_005269071.1:p.Val1342Gly
XM_006719493.1:c.4148T>G	XP_006719556.1:p.Val1383Gly
XM_006719494.1:c.4076T>G	XP_006719557.1:p.Val1359Gly
XM_006719496.1:c.4133T>G	XP_006719559.1:p.Val1378Gly
XM_011538556.1:c.4139T>G	XP_011536858.1:p.Val1380Gly
XM_005269007.3:c.4208T>G	XP_005269064.1:p.Val1403Gly
XM_005269008.3:c.4193T>G	XP_005269065.1:p.Val1398Gly
XM_005269009.3:c.4187T>G	XP_005269066.1:p.Val1396Gly
XM_005269010.3:c.4169T>G	XP_005269067.1:p.Val1390Gly
XM_005269011.3:c.4154T>G	XP_005269068.1:p.Val1385Gly
XM_005269012.3:c.4079T>G	XP_005269069.1:p.Val1360Gly
XM_005269013.3:c.4064T>G	XP_005269070.1:p.Val1355Gly
XM_005269014.3:c.4025T>G	XP_005269071.1:p.Val1342Gly
XM_006719493.3:c.4148T>G	XP_006719556.1:p.Val1383Gly
XM_006719494.3:c.4076T>G	XP_006719557.1:p.Val1359Gly
XM_011538556.3:c.4139T>G	XP_011536858.1:p.Val1380Gly
XM_017019607.2:c.4154T>G	XP_016875096.1:p.Val1385Gly
XM_017019608.2:c.4115T>G	XP_016875097.1:p.Val1372Gly
XM_017019609.2:c.4004T>G	XP_016875098.1:p.Val1335Gly
XM_017019610.2:c.4004T>G	XP_016875099.1:p.Val1335Gly
XM_017019611.2:c.3986T>G	XP_016875100.1:p.Val1329Gly
NM_001173463.2:c.4094T>G	NP_001166934.1:p.Val1365Gly
NM_001173464.2:c.4205T>G MANE Select	NP_001166935.1:p.Val1402Gly
NM_001173465.2:c.4046T>G	NP_001166936.1:p.Val1349Gly
NM_017641.4:c.4166T>G	NP_060111.2:p.Val1389Gly
NM_001378439.1:c.4208T>G	NP_001365368.1:p.Val1403Gly
NM_001378440.1:c.4193T>G	NP_001365369.1:p.Val1398Gly
NM_001378441.1:c.4169T>G	NP_001365370.1:p.Val1390Gly