Canonical Allele Identifier: CA384387387

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703493A>G (hg19) ; chr12:g.39309691A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309691A>G , CM000674.2:g.39309691A>G	GRCh38
NC_000012.11:g.39703493A>G , CM000674.1:g.39703493A>G	GRCh37
NC_000012.10:g.37989760A>G	NCBI36
NG_017067.1:g.138700T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4172T>C MANE Select	ENSP00000354878.5:p.Val1391Ala
ENST00000636569.1:c.4109T>C	ENSP00000490369.1:p.Val1370Ala
ENST00000361418.9:c.4172T>C	ENSP00000354878.5:p.Val1391Ala
ENST00000361961.7:c.4133T>C	ENSP00000354851.3:p.Val1378Ala
ENST00000541463.6:c.4013T>C	ENSP00000438075.2:p.Val1338Ala
ENST00000544797.6:c.4061T>C	ENSP00000445606.2:p.Val1354Ala
ENST00000547733.1:n.1486T>C
ENST00000551264.5:c.1115T>C	ENSP00000448792.1:p.Val372Ala
ENST00000552961.5:c.2074T>C
NM_001173463.1:c.4061T>C	NP_001166934.1:p.Val1354Ala
NM_001173464.1:c.4172T>C	NP_001166935.1:p.Val1391Ala
NM_001173465.1:c.4013T>C	NP_001166936.1:p.Val1338Ala
NM_017641.3:c.4133T>C	NP_060111.2:p.Val1378Ala
XM_005269007.1:c.4175T>C	XP_005269064.1:p.Val1392Ala
XM_005269008.1:c.4160T>C	XP_005269065.1:p.Val1387Ala
XM_005269009.1:c.4154T>C	XP_005269066.1:p.Val1385Ala
XM_005269010.1:c.4136T>C	XP_005269067.1:p.Val1379Ala
XM_005269011.1:c.4121T>C	XP_005269068.1:p.Val1374Ala
XM_005269012.1:c.4046T>C	XP_005269069.1:p.Val1349Ala
XM_005269013.1:c.4031T>C	XP_005269070.1:p.Val1344Ala
XM_005269014.1:c.3992T>C	XP_005269071.1:p.Val1331Ala
XM_006719493.1:c.4115T>C	XP_006719556.1:p.Val1372Ala
XM_006719494.1:c.4043T>C	XP_006719557.1:p.Val1348Ala
XM_006719496.1:c.4100T>C	XP_006719559.1:p.Val1367Ala
XM_011538556.1:c.4106T>C	XP_011536858.1:p.Val1369Ala
XM_005269007.3:c.4175T>C	XP_005269064.1:p.Val1392Ala
XM_005269008.3:c.4160T>C	XP_005269065.1:p.Val1387Ala
XM_005269009.3:c.4154T>C	XP_005269066.1:p.Val1385Ala
XM_005269010.3:c.4136T>C	XP_005269067.1:p.Val1379Ala
XM_005269011.3:c.4121T>C	XP_005269068.1:p.Val1374Ala
XM_005269012.3:c.4046T>C	XP_005269069.1:p.Val1349Ala
XM_005269013.3:c.4031T>C	XP_005269070.1:p.Val1344Ala
XM_005269014.3:c.3992T>C	XP_005269071.1:p.Val1331Ala
XM_006719493.3:c.4115T>C	XP_006719556.1:p.Val1372Ala
XM_006719494.3:c.4043T>C	XP_006719557.1:p.Val1348Ala
XM_011538556.3:c.4106T>C	XP_011536858.1:p.Val1369Ala
XM_017019607.2:c.4121T>C	XP_016875096.1:p.Val1374Ala
XM_017019608.2:c.4082T>C	XP_016875097.1:p.Val1361Ala
XM_017019609.2:c.3971T>C	XP_016875098.1:p.Val1324Ala
XM_017019610.2:c.3971T>C	XP_016875099.1:p.Val1324Ala
XM_017019611.2:c.3953T>C	XP_016875100.1:p.Val1318Ala
NM_001173463.2:c.4061T>C	NP_001166934.1:p.Val1354Ala
NM_001173464.2:c.4172T>C MANE Select	NP_001166935.1:p.Val1391Ala
NM_001173465.2:c.4013T>C	NP_001166936.1:p.Val1338Ala
NM_017641.4:c.4133T>C	NP_060111.2:p.Val1378Ala
NM_001378439.1:c.4175T>C	NP_001365368.1:p.Val1392Ala
NM_001378440.1:c.4160T>C	NP_001365369.1:p.Val1387Ala
NM_001378441.1:c.4136T>C	NP_001365370.1:p.Val1379Ala