Canonical Allele Identifier: CA384387440

Gene: KIF21A

Linked Data

• dbSNP Id: rs2137326172
• MyVariant Identifiers: chr12:g.39703500T>G (hg19) ; chr12:g.39309698T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309698T>G , CM000674.2:g.39309698T>G	GRCh38
NC_000012.11:g.39703500T>G , CM000674.1:g.39703500T>G	GRCh37
NC_000012.10:g.37989767T>G	NCBI36
NG_017067.1:g.138693A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4165A>C MANE Select	ENSP00000354878.5:p.Asn1389His
ENST00000636569.1:c.4102A>C	ENSP00000490369.1:p.Asn1368His
ENST00000361418.9:c.4165A>C	ENSP00000354878.5:p.Asn1389His
ENST00000361961.7:c.4126A>C	ENSP00000354851.3:p.Asn1376His
ENST00000541463.6:c.4006A>C	ENSP00000438075.2:p.Asn1336His
ENST00000544797.6:c.4054A>C	ENSP00000445606.2:p.Asn1352His
ENST00000547733.1:n.1479A>C
ENST00000551264.5:c.1108A>C	ENSP00000448792.1:p.Asn370His
ENST00000552961.5:c.2067A>C
NM_001173463.1:c.4054A>C	NP_001166934.1:p.Asn1352His
NM_001173464.1:c.4165A>C	NP_001166935.1:p.Asn1389His
NM_001173465.1:c.4006A>C	NP_001166936.1:p.Asn1336His
NM_017641.3:c.4126A>C	NP_060111.2:p.Asn1376His
XM_005269007.1:c.4168A>C	XP_005269064.1:p.Asn1390His
XM_005269008.1:c.4153A>C	XP_005269065.1:p.Asn1385His
XM_005269009.1:c.4147A>C	XP_005269066.1:p.Asn1383His
XM_005269010.1:c.4129A>C	XP_005269067.1:p.Asn1377His
XM_005269011.1:c.4114A>C	XP_005269068.1:p.Asn1372His
XM_005269012.1:c.4039A>C	XP_005269069.1:p.Asn1347His
XM_005269013.1:c.4024A>C	XP_005269070.1:p.Asn1342His
XM_005269014.1:c.3985A>C	XP_005269071.1:p.Asn1329His
XM_006719493.1:c.4108A>C	XP_006719556.1:p.Asn1370His
XM_006719494.1:c.4036A>C	XP_006719557.1:p.Asn1346His
XM_006719496.1:c.4093A>C	XP_006719559.1:p.Asn1365His
XM_011538556.1:c.4099A>C	XP_011536858.1:p.Asn1367His
XM_005269007.3:c.4168A>C	XP_005269064.1:p.Asn1390His
XM_005269008.3:c.4153A>C	XP_005269065.1:p.Asn1385His
XM_005269009.3:c.4147A>C	XP_005269066.1:p.Asn1383His
XM_005269010.3:c.4129A>C	XP_005269067.1:p.Asn1377His
XM_005269011.3:c.4114A>C	XP_005269068.1:p.Asn1372His
XM_005269012.3:c.4039A>C	XP_005269069.1:p.Asn1347His
XM_005269013.3:c.4024A>C	XP_005269070.1:p.Asn1342His
XM_005269014.3:c.3985A>C	XP_005269071.1:p.Asn1329His
XM_006719493.3:c.4108A>C	XP_006719556.1:p.Asn1370His
XM_006719494.3:c.4036A>C	XP_006719557.1:p.Asn1346His
XM_011538556.3:c.4099A>C	XP_011536858.1:p.Asn1367His
XM_017019607.2:c.4114A>C	XP_016875096.1:p.Asn1372His
XM_017019608.2:c.4075A>C	XP_016875097.1:p.Asn1359His
XM_017019609.2:c.3964A>C	XP_016875098.1:p.Asn1322His
XM_017019610.2:c.3964A>C	XP_016875099.1:p.Asn1322His
XM_017019611.2:c.3946A>C	XP_016875100.1:p.Asn1316His
NM_001173463.2:c.4054A>C	NP_001166934.1:p.Asn1352His
NM_001173464.2:c.4165A>C MANE Select	NP_001166935.1:p.Asn1389His
NM_001173465.2:c.4006A>C	NP_001166936.1:p.Asn1336His
NM_017641.4:c.4126A>C	NP_060111.2:p.Asn1376His
NM_001378439.1:c.4168A>C	NP_001365368.1:p.Asn1390His
NM_001378440.1:c.4153A>C	NP_001365369.1:p.Asn1385His
NM_001378441.1:c.4129A>C	NP_001365370.1:p.Asn1377His