Canonical Allele Identifier: CA384386797

Gene: KIF21A

Linked Data

• MyVariant Identifiers: chr12:g.39703402G>C (hg19) ; chr12:g.39309600G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.39309600G>C , CM000674.2:g.39309600G>C	GRCh38
NC_000012.11:g.39703402G>C , CM000674.1:g.39703402G>C	GRCh37
NC_000012.10:g.37989669G>C	NCBI36
NG_017067.1:g.138791C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361418.10:c.4263C>G MANE Select	ENSP00000354878.5:p.Cys1421Trp
ENST00000636569.1:c.4200C>G	ENSP00000490369.1:p.Cys1400Trp
ENST00000361418.9:c.4263C>G	ENSP00000354878.5:p.Cys1421Trp
ENST00000361961.7:c.4224C>G	ENSP00000354851.3:p.Cys1408Trp
ENST00000541463.6:c.4104C>G	ENSP00000438075.2:p.Cys1368Trp
ENST00000544797.6:c.4152C>G	ENSP00000445606.2:p.Cys1384Trp
ENST00000547733.1:n.1577C>G
ENST00000551264.5:c.1206C>G	ENSP00000448792.1:p.Cys402Trp
ENST00000552961.5:c.2165C>G
NM_001173463.1:c.4152C>G	NP_001166934.1:p.Cys1384Trp
NM_001173464.1:c.4263C>G	NP_001166935.1:p.Cys1421Trp
NM_001173465.1:c.4104C>G	NP_001166936.1:p.Cys1368Trp
NM_017641.3:c.4224C>G	NP_060111.2:p.Cys1408Trp
XM_005269007.1:c.4266C>G	XP_005269064.1:p.Cys1422Trp
XM_005269008.1:c.4251C>G	XP_005269065.1:p.Cys1417Trp
XM_005269009.1:c.4245C>G	XP_005269066.1:p.Cys1415Trp
XM_005269010.1:c.4227C>G	XP_005269067.1:p.Cys1409Trp
XM_005269011.1:c.4212C>G	XP_005269068.1:p.Cys1404Trp
XM_005269012.1:c.4137C>G	XP_005269069.1:p.Cys1379Trp
XM_005269013.1:c.4122C>G	XP_005269070.1:p.Cys1374Trp
XM_005269014.1:c.4083C>G	XP_005269071.1:p.Cys1361Trp
XM_006719493.1:c.4206C>G	XP_006719556.1:p.Cys1402Trp
XM_006719494.1:c.4134C>G	XP_006719557.1:p.Cys1378Trp
XM_006719496.1:c.4191C>G	XP_006719559.1:p.Cys1397Trp
XM_011538556.1:c.4197C>G	XP_011536858.1:p.Cys1399Trp
XM_005269007.3:c.4266C>G	XP_005269064.1:p.Cys1422Trp
XM_005269008.3:c.4251C>G	XP_005269065.1:p.Cys1417Trp
XM_005269009.3:c.4245C>G	XP_005269066.1:p.Cys1415Trp
XM_005269010.3:c.4227C>G	XP_005269067.1:p.Cys1409Trp
XM_005269011.3:c.4212C>G	XP_005269068.1:p.Cys1404Trp
XM_005269012.3:c.4137C>G	XP_005269069.1:p.Cys1379Trp
XM_005269013.3:c.4122C>G	XP_005269070.1:p.Cys1374Trp
XM_005269014.3:c.4083C>G	XP_005269071.1:p.Cys1361Trp
XM_006719493.3:c.4206C>G	XP_006719556.1:p.Cys1402Trp
XM_006719494.3:c.4134C>G	XP_006719557.1:p.Cys1378Trp
XM_011538556.3:c.4197C>G	XP_011536858.1:p.Cys1399Trp
XM_017019607.2:c.4212C>G	XP_016875096.1:p.Cys1404Trp
XM_017019608.2:c.4173C>G	XP_016875097.1:p.Cys1391Trp
XM_017019609.2:c.4062C>G	XP_016875098.1:p.Cys1354Trp
XM_017019610.2:c.4062C>G	XP_016875099.1:p.Cys1354Trp
XM_017019611.2:c.4044C>G	XP_016875100.1:p.Cys1348Trp
NM_001173463.2:c.4152C>G	NP_001166934.1:p.Cys1384Trp
NM_001173464.2:c.4263C>G MANE Select	NP_001166935.1:p.Cys1421Trp
NM_001173465.2:c.4104C>G	NP_001166936.1:p.Cys1368Trp
NM_017641.4:c.4224C>G	NP_060111.2:p.Cys1408Trp
NM_001378439.1:c.4266C>G	NP_001365368.1:p.Cys1422Trp
NM_001378440.1:c.4251C>G	NP_001365369.1:p.Cys1417Trp
NM_001378441.1:c.4227C>G	NP_001365370.1:p.Cys1409Trp