Canonical Allele Identifier: CA384387401

Gene: KIF21A

Linked Data

• gnomAD v4: 12-39309694-A-T
• MyVariant Identifiers: chr12:g.39703496A>T (hg19) ; chr12:g.39309694A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309694A>T , CM000674.2:g.39309694A>T	GRCh38
NC_000012.11:g.39703496A>T , CM000674.1:g.39703496A>T	GRCh37
NC_000012.10:g.37989763A>T	NCBI36
NG_017067.1:g.138697T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4169T>A MANE Select	ENSP00000354878.5:p.Val1390Asp
ENST00000636569.1:c.4106T>A	ENSP00000490369.1:p.Val1369Asp
ENST00000361418.9:c.4169T>A	ENSP00000354878.5:p.Val1390Asp
ENST00000361961.7:c.4130T>A	ENSP00000354851.3:p.Val1377Asp
ENST00000541463.6:c.4010T>A	ENSP00000438075.2:p.Val1337Asp
ENST00000544797.6:c.4058T>A	ENSP00000445606.2:p.Val1353Asp
ENST00000547733.1:n.1483T>A
ENST00000551264.5:c.1112T>A	ENSP00000448792.1:p.Val371Asp
ENST00000552961.5:c.2071T>A
NM_001173463.1:c.4058T>A	NP_001166934.1:p.Val1353Asp
NM_001173464.1:c.4169T>A	NP_001166935.1:p.Val1390Asp
NM_001173465.1:c.4010T>A	NP_001166936.1:p.Val1337Asp
NM_017641.3:c.4130T>A	NP_060111.2:p.Val1377Asp
XM_005269007.1:c.4172T>A	XP_005269064.1:p.Val1391Asp
XM_005269008.1:c.4157T>A	XP_005269065.1:p.Val1386Asp
XM_005269009.1:c.4151T>A	XP_005269066.1:p.Val1384Asp
XM_005269010.1:c.4133T>A	XP_005269067.1:p.Val1378Asp
XM_005269011.1:c.4118T>A	XP_005269068.1:p.Val1373Asp
XM_005269012.1:c.4043T>A	XP_005269069.1:p.Val1348Asp
XM_005269013.1:c.4028T>A	XP_005269070.1:p.Val1343Asp
XM_005269014.1:c.3989T>A	XP_005269071.1:p.Val1330Asp
XM_006719493.1:c.4112T>A	XP_006719556.1:p.Val1371Asp
XM_006719494.1:c.4040T>A	XP_006719557.1:p.Val1347Asp
XM_006719496.1:c.4097T>A	XP_006719559.1:p.Val1366Asp
XM_011538556.1:c.4103T>A	XP_011536858.1:p.Val1368Asp
XM_005269007.3:c.4172T>A	XP_005269064.1:p.Val1391Asp
XM_005269008.3:c.4157T>A	XP_005269065.1:p.Val1386Asp
XM_005269009.3:c.4151T>A	XP_005269066.1:p.Val1384Asp
XM_005269010.3:c.4133T>A	XP_005269067.1:p.Val1378Asp
XM_005269011.3:c.4118T>A	XP_005269068.1:p.Val1373Asp
XM_005269012.3:c.4043T>A	XP_005269069.1:p.Val1348Asp
XM_005269013.3:c.4028T>A	XP_005269070.1:p.Val1343Asp
XM_005269014.3:c.3989T>A	XP_005269071.1:p.Val1330Asp
XM_006719493.3:c.4112T>A	XP_006719556.1:p.Val1371Asp
XM_006719494.3:c.4040T>A	XP_006719557.1:p.Val1347Asp
XM_011538556.3:c.4103T>A	XP_011536858.1:p.Val1368Asp
XM_017019607.2:c.4118T>A	XP_016875096.1:p.Val1373Asp
XM_017019608.2:c.4079T>A	XP_016875097.1:p.Val1360Asp
XM_017019609.2:c.3968T>A	XP_016875098.1:p.Val1323Asp
XM_017019610.2:c.3968T>A	XP_016875099.1:p.Val1323Asp
XM_017019611.2:c.3950T>A	XP_016875100.1:p.Val1317Asp
NM_001173463.2:c.4058T>A	NP_001166934.1:p.Val1353Asp
NM_001173464.2:c.4169T>A MANE Select	NP_001166935.1:p.Val1390Asp
NM_001173465.2:c.4010T>A	NP_001166936.1:p.Val1337Asp
NM_017641.4:c.4130T>A	NP_060111.2:p.Val1377Asp
NM_001378439.1:c.4172T>A	NP_001365368.1:p.Val1391Asp
NM_001378440.1:c.4157T>A	NP_001365369.1:p.Val1386Asp
NM_001378441.1:c.4133T>A	NP_001365370.1:p.Val1378Asp