Canonical Allele Identifier: CA384386887

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703416C>A (hg19) ; chr12:g.39309614C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309614C>A , CM000674.2:g.39309614C>A	GRCh38
NC_000012.11:g.39703416C>A , CM000674.1:g.39703416C>A	GRCh37
NC_000012.10:g.37989683C>A	NCBI36
NG_017067.1:g.138777G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4249G>T MANE Select	ENSP00000354878.5:p.Asp1417Tyr
ENST00000636569.1:c.4186G>T	ENSP00000490369.1:p.Asp1396Tyr
ENST00000361418.9:c.4249G>T	ENSP00000354878.5:p.Asp1417Tyr
ENST00000361961.7:c.4210G>T	ENSP00000354851.3:p.Asp1404Tyr
ENST00000541463.6:c.4090G>T	ENSP00000438075.2:p.Asp1364Tyr
ENST00000544797.6:c.4138G>T	ENSP00000445606.2:p.Asp1380Tyr
ENST00000547733.1:n.1563G>T
ENST00000551264.5:c.1192G>T	ENSP00000448792.1:p.Asp398Tyr
ENST00000552961.5:c.2151G>T
NM_001173463.1:c.4138G>T	NP_001166934.1:p.Asp1380Tyr
NM_001173464.1:c.4249G>T	NP_001166935.1:p.Asp1417Tyr
NM_001173465.1:c.4090G>T	NP_001166936.1:p.Asp1364Tyr
NM_017641.3:c.4210G>T	NP_060111.2:p.Asp1404Tyr
XM_005269007.1:c.4252G>T	XP_005269064.1:p.Asp1418Tyr
XM_005269008.1:c.4237G>T	XP_005269065.1:p.Asp1413Tyr
XM_005269009.1:c.4231G>T	XP_005269066.1:p.Asp1411Tyr
XM_005269010.1:c.4213G>T	XP_005269067.1:p.Asp1405Tyr
XM_005269011.1:c.4198G>T	XP_005269068.1:p.Asp1400Tyr
XM_005269012.1:c.4123G>T	XP_005269069.1:p.Asp1375Tyr
XM_005269013.1:c.4108G>T	XP_005269070.1:p.Asp1370Tyr
XM_005269014.1:c.4069G>T	XP_005269071.1:p.Asp1357Tyr
XM_006719493.1:c.4192G>T	XP_006719556.1:p.Asp1398Tyr
XM_006719494.1:c.4120G>T	XP_006719557.1:p.Asp1374Tyr
XM_006719496.1:c.4177G>T	XP_006719559.1:p.Asp1393Tyr
XM_011538556.1:c.4183G>T	XP_011536858.1:p.Asp1395Tyr
XM_005269007.3:c.4252G>T	XP_005269064.1:p.Asp1418Tyr
XM_005269008.3:c.4237G>T	XP_005269065.1:p.Asp1413Tyr
XM_005269009.3:c.4231G>T	XP_005269066.1:p.Asp1411Tyr
XM_005269010.3:c.4213G>T	XP_005269067.1:p.Asp1405Tyr
XM_005269011.3:c.4198G>T	XP_005269068.1:p.Asp1400Tyr
XM_005269012.3:c.4123G>T	XP_005269069.1:p.Asp1375Tyr
XM_005269013.3:c.4108G>T	XP_005269070.1:p.Asp1370Tyr
XM_005269014.3:c.4069G>T	XP_005269071.1:p.Asp1357Tyr
XM_006719493.3:c.4192G>T	XP_006719556.1:p.Asp1398Tyr
XM_006719494.3:c.4120G>T	XP_006719557.1:p.Asp1374Tyr
XM_011538556.3:c.4183G>T	XP_011536858.1:p.Asp1395Tyr
XM_017019607.2:c.4198G>T	XP_016875096.1:p.Asp1400Tyr
XM_017019608.2:c.4159G>T	XP_016875097.1:p.Asp1387Tyr
XM_017019609.2:c.4048G>T	XP_016875098.1:p.Asp1350Tyr
XM_017019610.2:c.4048G>T	XP_016875099.1:p.Asp1350Tyr
XM_017019611.2:c.4030G>T	XP_016875100.1:p.Asp1344Tyr
NM_001173463.2:c.4138G>T	NP_001166934.1:p.Asp1380Tyr
NM_001173464.2:c.4249G>T MANE Select	NP_001166935.1:p.Asp1417Tyr
NM_001173465.2:c.4090G>T	NP_001166936.1:p.Asp1364Tyr
NM_017641.4:c.4210G>T	NP_060111.2:p.Asp1404Tyr
NM_001378439.1:c.4252G>T	NP_001365368.1:p.Asp1418Tyr
NM_001378440.1:c.4237G>T	NP_001365369.1:p.Asp1413Tyr
NM_001378441.1:c.4213G>T	NP_001365370.1:p.Asp1405Tyr