Canonical Allele Identifier: CA384386956

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703425C>T (hg19) ; chr12:g.39309623C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309623C>T , CM000674.2:g.39309623C>T	GRCh38
NC_000012.11:g.39703425C>T , CM000674.1:g.39703425C>T	GRCh37
NC_000012.10:g.37989692C>T	NCBI36
NG_017067.1:g.138768G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4240G>A MANE Select	ENSP00000354878.5:p.Asp1414Asn
ENST00000636569.1:c.4177G>A	ENSP00000490369.1:p.Asp1393Asn
ENST00000361418.9:c.4240G>A	ENSP00000354878.5:p.Asp1414Asn
ENST00000361961.7:c.4201G>A	ENSP00000354851.3:p.Asp1401Asn
ENST00000541463.6:c.4081G>A	ENSP00000438075.2:p.Asp1361Asn
ENST00000544797.6:c.4129G>A	ENSP00000445606.2:p.Asp1377Asn
ENST00000547733.1:n.1554G>A
ENST00000551264.5:c.1183G>A	ENSP00000448792.1:p.Asp395Asn
ENST00000552961.5:c.2142G>A
NM_001173463.1:c.4129G>A	NP_001166934.1:p.Asp1377Asn
NM_001173464.1:c.4240G>A	NP_001166935.1:p.Asp1414Asn
NM_001173465.1:c.4081G>A	NP_001166936.1:p.Asp1361Asn
NM_017641.3:c.4201G>A	NP_060111.2:p.Asp1401Asn
XM_005269007.1:c.4243G>A	XP_005269064.1:p.Asp1415Asn
XM_005269008.1:c.4228G>A	XP_005269065.1:p.Asp1410Asn
XM_005269009.1:c.4222G>A	XP_005269066.1:p.Asp1408Asn
XM_005269010.1:c.4204G>A	XP_005269067.1:p.Asp1402Asn
XM_005269011.1:c.4189G>A	XP_005269068.1:p.Asp1397Asn
XM_005269012.1:c.4114G>A	XP_005269069.1:p.Asp1372Asn
XM_005269013.1:c.4099G>A	XP_005269070.1:p.Asp1367Asn
XM_005269014.1:c.4060G>A	XP_005269071.1:p.Asp1354Asn
XM_006719493.1:c.4183G>A	XP_006719556.1:p.Asp1395Asn
XM_006719494.1:c.4111G>A	XP_006719557.1:p.Asp1371Asn
XM_006719496.1:c.4168G>A	XP_006719559.1:p.Asp1390Asn
XM_011538556.1:c.4174G>A	XP_011536858.1:p.Asp1392Asn
XM_005269007.3:c.4243G>A	XP_005269064.1:p.Asp1415Asn
XM_005269008.3:c.4228G>A	XP_005269065.1:p.Asp1410Asn
XM_005269009.3:c.4222G>A	XP_005269066.1:p.Asp1408Asn
XM_005269010.3:c.4204G>A	XP_005269067.1:p.Asp1402Asn
XM_005269011.3:c.4189G>A	XP_005269068.1:p.Asp1397Asn
XM_005269012.3:c.4114G>A	XP_005269069.1:p.Asp1372Asn
XM_005269013.3:c.4099G>A	XP_005269070.1:p.Asp1367Asn
XM_005269014.3:c.4060G>A	XP_005269071.1:p.Asp1354Asn
XM_006719493.3:c.4183G>A	XP_006719556.1:p.Asp1395Asn
XM_006719494.3:c.4111G>A	XP_006719557.1:p.Asp1371Asn
XM_011538556.3:c.4174G>A	XP_011536858.1:p.Asp1392Asn
XM_017019607.2:c.4189G>A	XP_016875096.1:p.Asp1397Asn
XM_017019608.2:c.4150G>A	XP_016875097.1:p.Asp1384Asn
XM_017019609.2:c.4039G>A	XP_016875098.1:p.Asp1347Asn
XM_017019610.2:c.4039G>A	XP_016875099.1:p.Asp1347Asn
XM_017019611.2:c.4021G>A	XP_016875100.1:p.Asp1341Asn
NM_001173463.2:c.4129G>A	NP_001166934.1:p.Asp1377Asn
NM_001173464.2:c.4240G>A MANE Select	NP_001166935.1:p.Asp1414Asn
NM_001173465.2:c.4081G>A	NP_001166936.1:p.Asp1361Asn
NM_017641.4:c.4201G>A	NP_060111.2:p.Asp1401Asn
NM_001378439.1:c.4243G>A	NP_001365368.1:p.Asp1415Asn
NM_001378440.1:c.4228G>A	NP_001365369.1:p.Asp1410Asn
NM_001378441.1:c.4204G>A	NP_001365370.1:p.Asp1402Asn