Canonical Allele Identifier: CA384387271

Gene: KIF21A

Linked Data

• dbSNP Id: rs1202745618
• gnomAD v2: 12-39703476-T-C
• gnomAD v4: 12-39309674-T-C
• MyVariant Identifiers: chr12:g.39703476T>C (hg19) ; chr12:g.39309674T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309674T>C , CM000674.2:g.39309674T>C	GRCh38
NC_000012.11:g.39703476T>C , CM000674.1:g.39703476T>C	GRCh37
NC_000012.10:g.37989743T>C	NCBI36
NG_017067.1:g.138717A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4189A>G MANE Select	ENSP00000354878.5:p.Asn1397Asp
ENST00000636569.1:c.4126A>G	ENSP00000490369.1:p.Asn1376Asp
ENST00000361418.9:c.4189A>G	ENSP00000354878.5:p.Asn1397Asp
ENST00000361961.7:c.4150A>G	ENSP00000354851.3:p.Asn1384Asp
ENST00000541463.6:c.4030A>G	ENSP00000438075.2:p.Asn1344Asp
ENST00000544797.6:c.4078A>G	ENSP00000445606.2:p.Asn1360Asp
ENST00000547733.1:n.1503A>G
ENST00000551264.5:c.1132A>G	ENSP00000448792.1:p.Asn378Asp
ENST00000552961.5:c.2091A>G
NM_001173463.1:c.4078A>G	NP_001166934.1:p.Asn1360Asp
NM_001173464.1:c.4189A>G	NP_001166935.1:p.Asn1397Asp
NM_001173465.1:c.4030A>G	NP_001166936.1:p.Asn1344Asp
NM_017641.3:c.4150A>G	NP_060111.2:p.Asn1384Asp
XM_005269007.1:c.4192A>G	XP_005269064.1:p.Asn1398Asp
XM_005269008.1:c.4177A>G	XP_005269065.1:p.Asn1393Asp
XM_005269009.1:c.4171A>G	XP_005269066.1:p.Asn1391Asp
XM_005269010.1:c.4153A>G	XP_005269067.1:p.Asn1385Asp
XM_005269011.1:c.4138A>G	XP_005269068.1:p.Asn1380Asp
XM_005269012.1:c.4063A>G	XP_005269069.1:p.Asn1355Asp
XM_005269013.1:c.4048A>G	XP_005269070.1:p.Asn1350Asp
XM_005269014.1:c.4009A>G	XP_005269071.1:p.Asn1337Asp
XM_006719493.1:c.4132A>G	XP_006719556.1:p.Asn1378Asp
XM_006719494.1:c.4060A>G	XP_006719557.1:p.Asn1354Asp
XM_006719496.1:c.4117A>G	XP_006719559.1:p.Asn1373Asp
XM_011538556.1:c.4123A>G	XP_011536858.1:p.Asn1375Asp
XM_005269007.3:c.4192A>G	XP_005269064.1:p.Asn1398Asp
XM_005269008.3:c.4177A>G	XP_005269065.1:p.Asn1393Asp
XM_005269009.3:c.4171A>G	XP_005269066.1:p.Asn1391Asp
XM_005269010.3:c.4153A>G	XP_005269067.1:p.Asn1385Asp
XM_005269011.3:c.4138A>G	XP_005269068.1:p.Asn1380Asp
XM_005269012.3:c.4063A>G	XP_005269069.1:p.Asn1355Asp
XM_005269013.3:c.4048A>G	XP_005269070.1:p.Asn1350Asp
XM_005269014.3:c.4009A>G	XP_005269071.1:p.Asn1337Asp
XM_006719493.3:c.4132A>G	XP_006719556.1:p.Asn1378Asp
XM_006719494.3:c.4060A>G	XP_006719557.1:p.Asn1354Asp
XM_011538556.3:c.4123A>G	XP_011536858.1:p.Asn1375Asp
XM_017019607.2:c.4138A>G	XP_016875096.1:p.Asn1380Asp
XM_017019608.2:c.4099A>G	XP_016875097.1:p.Asn1367Asp
XM_017019609.2:c.3988A>G	XP_016875098.1:p.Asn1330Asp
XM_017019610.2:c.3988A>G	XP_016875099.1:p.Asn1330Asp
XM_017019611.2:c.3970A>G	XP_016875100.1:p.Asn1324Asp
NM_001173463.2:c.4078A>G	NP_001166934.1:p.Asn1360Asp
NM_001173464.2:c.4189A>G MANE Select	NP_001166935.1:p.Asn1397Asp
NM_001173465.2:c.4030A>G	NP_001166936.1:p.Asn1344Asp
NM_017641.4:c.4150A>G	NP_060111.2:p.Asn1384Asp
NM_001378439.1:c.4192A>G	NP_001365368.1:p.Asn1398Asp
NM_001378440.1:c.4177A>G	NP_001365369.1:p.Asn1393Asp
NM_001378441.1:c.4153A>G	NP_001365370.1:p.Asn1385Asp