Canonical Allele Identifier: CA384386788

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703400A>T (hg19) ; chr12:g.39309598A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309598A>T , CM000674.2:g.39309598A>T	GRCh38
NC_000012.11:g.39703400A>T , CM000674.1:g.39703400A>T	GRCh37
NC_000012.10:g.37989667A>T	NCBI36
NG_017067.1:g.138793T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000361418.10:c.4265T>A MANE Select	ENSP00000354878.5:p.Ile1422Asn
ENST00000636569.1:c.4202T>A	ENSP00000490369.1:p.Ile1401Asn
ENST00000361418.9:c.4265T>A	ENSP00000354878.5:p.Ile1422Asn
ENST00000361961.7:c.4226T>A	ENSP00000354851.3:p.Ile1409Asn
ENST00000541463.6:c.4106T>A	ENSP00000438075.2:p.Ile1369Asn
ENST00000544797.6:c.4154T>A	ENSP00000445606.2:p.Ile1385Asn
ENST00000547733.1:n.1579T>A
ENST00000551264.5:c.1208T>A	ENSP00000448792.1:p.Ile403Asn
ENST00000552961.5:c.2167T>A
NM_001173463.1:c.4154T>A	NP_001166934.1:p.Ile1385Asn
NM_001173464.1:c.4265T>A	NP_001166935.1:p.Ile1422Asn
NM_001173465.1:c.4106T>A	NP_001166936.1:p.Ile1369Asn
NM_017641.3:c.4226T>A	NP_060111.2:p.Ile1409Asn
XM_005269007.1:c.4268T>A	XP_005269064.1:p.Ile1423Asn
XM_005269008.1:c.4253T>A	XP_005269065.1:p.Ile1418Asn
XM_005269009.1:c.4247T>A	XP_005269066.1:p.Ile1416Asn
XM_005269010.1:c.4229T>A	XP_005269067.1:p.Ile1410Asn
XM_005269011.1:c.4214T>A	XP_005269068.1:p.Ile1405Asn
XM_005269012.1:c.4139T>A	XP_005269069.1:p.Ile1380Asn
XM_005269013.1:c.4124T>A	XP_005269070.1:p.Ile1375Asn
XM_005269014.1:c.4085T>A	XP_005269071.1:p.Ile1362Asn
XM_006719493.1:c.4208T>A	XP_006719556.1:p.Ile1403Asn
XM_006719494.1:c.4136T>A	XP_006719557.1:p.Ile1379Asn
XM_006719496.1:c.4193T>A	XP_006719559.1:p.Ile1398Asn
XM_011538556.1:c.4199T>A	XP_011536858.1:p.Ile1400Asn
XM_005269007.3:c.4268T>A	XP_005269064.1:p.Ile1423Asn
XM_005269008.3:c.4253T>A	XP_005269065.1:p.Ile1418Asn
XM_005269009.3:c.4247T>A	XP_005269066.1:p.Ile1416Asn
XM_005269010.3:c.4229T>A	XP_005269067.1:p.Ile1410Asn
XM_005269011.3:c.4214T>A	XP_005269068.1:p.Ile1405Asn
XM_005269012.3:c.4139T>A	XP_005269069.1:p.Ile1380Asn
XM_005269013.3:c.4124T>A	XP_005269070.1:p.Ile1375Asn
XM_005269014.3:c.4085T>A	XP_005269071.1:p.Ile1362Asn
XM_006719493.3:c.4208T>A	XP_006719556.1:p.Ile1403Asn
XM_006719494.3:c.4136T>A	XP_006719557.1:p.Ile1379Asn
XM_011538556.3:c.4199T>A	XP_011536858.1:p.Ile1400Asn
XM_017019607.2:c.4214T>A	XP_016875096.1:p.Ile1405Asn
XM_017019608.2:c.4175T>A	XP_016875097.1:p.Ile1392Asn
XM_017019609.2:c.4064T>A	XP_016875098.1:p.Ile1355Asn
XM_017019610.2:c.4064T>A	XP_016875099.1:p.Ile1355Asn
XM_017019611.2:c.4046T>A	XP_016875100.1:p.Ile1349Asn
NM_001173463.2:c.4154T>A	NP_001166934.1:p.Ile1385Asn
NM_001173464.2:c.4265T>A MANE Select	NP_001166935.1:p.Ile1422Asn
NM_001173465.2:c.4106T>A	NP_001166936.1:p.Ile1369Asn
NM_017641.4:c.4226T>A	NP_060111.2:p.Ile1409Asn
NM_001378439.1:c.4268T>A	NP_001365368.1:p.Ile1423Asn
NM_001378440.1:c.4253T>A	NP_001365369.1:p.Ile1418Asn
NM_001378441.1:c.4229T>A	NP_001365370.1:p.Ile1410Asn