Canonical Allele Identifier: CA384386780

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703398G>C (hg19) ; chr12:g.39309596G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309596G>C , CM000674.2:g.39309596G>C	GRCh38
NC_000012.11:g.39703398G>C , CM000674.1:g.39703398G>C	GRCh37
NC_000012.10:g.37989665G>C	NCBI36
NG_017067.1:g.138795C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000361418.10:c.4267C>G MANE Select	ENSP00000354878.5:p.Arg1423Gly
ENST00000636569.1:c.4204C>G	ENSP00000490369.1:p.Arg1402Gly
ENST00000361418.9:c.4267C>G	ENSP00000354878.5:p.Arg1423Gly
ENST00000361961.7:c.4228C>G	ENSP00000354851.3:p.Arg1410Gly
ENST00000541463.6:c.4108C>G	ENSP00000438075.2:p.Arg1370Gly
ENST00000544797.6:c.4156C>G	ENSP00000445606.2:p.Arg1386Gly
ENST00000547733.1:n.1581C>G
ENST00000551264.5:c.1210C>G	ENSP00000448792.1:p.Arg404Gly
ENST00000552961.5:c.2169C>G
NM_001173463.1:c.4156C>G	NP_001166934.1:p.Arg1386Gly
NM_001173464.1:c.4267C>G	NP_001166935.1:p.Arg1423Gly
NM_001173465.1:c.4108C>G	NP_001166936.1:p.Arg1370Gly
NM_017641.3:c.4228C>G	NP_060111.2:p.Arg1410Gly
XM_005269007.1:c.4270C>G	XP_005269064.1:p.Arg1424Gly
XM_005269008.1:c.4255C>G	XP_005269065.1:p.Arg1419Gly
XM_005269009.1:c.4249C>G	XP_005269066.1:p.Arg1417Gly
XM_005269010.1:c.4231C>G	XP_005269067.1:p.Arg1411Gly
XM_005269011.1:c.4216C>G	XP_005269068.1:p.Arg1406Gly
XM_005269012.1:c.4141C>G	XP_005269069.1:p.Arg1381Gly
XM_005269013.1:c.4126C>G	XP_005269070.1:p.Arg1376Gly
XM_005269014.1:c.4087C>G	XP_005269071.1:p.Arg1363Gly
XM_006719493.1:c.4210C>G	XP_006719556.1:p.Arg1404Gly
XM_006719494.1:c.4138C>G	XP_006719557.1:p.Arg1380Gly
XM_006719496.1:c.4195C>G	XP_006719559.1:p.Arg1399Gly
XM_011538556.1:c.4201C>G	XP_011536858.1:p.Arg1401Gly
XM_005269007.3:c.4270C>G	XP_005269064.1:p.Arg1424Gly
XM_005269008.3:c.4255C>G	XP_005269065.1:p.Arg1419Gly
XM_005269009.3:c.4249C>G	XP_005269066.1:p.Arg1417Gly
XM_005269010.3:c.4231C>G	XP_005269067.1:p.Arg1411Gly
XM_005269011.3:c.4216C>G	XP_005269068.1:p.Arg1406Gly
XM_005269012.3:c.4141C>G	XP_005269069.1:p.Arg1381Gly
XM_005269013.3:c.4126C>G	XP_005269070.1:p.Arg1376Gly
XM_005269014.3:c.4087C>G	XP_005269071.1:p.Arg1363Gly
XM_006719493.3:c.4210C>G	XP_006719556.1:p.Arg1404Gly
XM_006719494.3:c.4138C>G	XP_006719557.1:p.Arg1380Gly
XM_011538556.3:c.4201C>G	XP_011536858.1:p.Arg1401Gly
XM_017019607.2:c.4216C>G	XP_016875096.1:p.Arg1406Gly
XM_017019608.2:c.4177C>G	XP_016875097.1:p.Arg1393Gly
XM_017019609.2:c.4066C>G	XP_016875098.1:p.Arg1356Gly
XM_017019610.2:c.4066C>G	XP_016875099.1:p.Arg1356Gly
XM_017019611.2:c.4048C>G	XP_016875100.1:p.Arg1350Gly
NM_001173463.2:c.4156C>G	NP_001166934.1:p.Arg1386Gly
NM_001173464.2:c.4267C>G MANE Select	NP_001166935.1:p.Arg1423Gly
NM_001173465.2:c.4108C>G	NP_001166936.1:p.Arg1370Gly
NM_017641.4:c.4228C>G	NP_060111.2:p.Arg1410Gly
NM_001378439.1:c.4270C>G	NP_001365368.1:p.Arg1424Gly
NM_001378440.1:c.4255C>G	NP_001365369.1:p.Arg1419Gly
NM_001378441.1:c.4231C>G	NP_001365370.1:p.Arg1411Gly