Canonical Allele Identifier: CA115556
Gene: KIF21A HGNC NCBI

Linked Data

ClinVar Variation Id: 2442
ClinVar RCV Id: RCV000002546
dbSNP Id: rs267607200

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.39332606C>T , CM000674.2:g.39332606C>T GRCh38
NC_000012.11:g.39726408C>T , CM000674.1:g.39726408C>T GRCh37
NC_000012.10:g.38012675C>T NCBI36
NG_017067.1:g.115785G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000361418.10:c.2841G>A MANE Select ENSP00000354878.5:p.Met947Ile
ENST00000636569.1:c.2775G>A ENSP00000490369.1:p.Met925Ile
ENST00000361418.9:c.2841G>A ENSP00000354878.5:p.Met947Ile
ENST00000361961.7:c.2802G>A ENSP00000354851.3:p.Met934Ile
ENST00000541463.6:c.2733G>A ENSP00000438075.2:p.Met911Ile
ENST00000544797.6:c.2802G>A ENSP00000445606.2:p.Met934Ile
ENST00000547108.5:c.614G>A
ENST00000552961.5:c.884G>A
NM_001173463.1:c.2802G>A NP_001166934.1:p.Met934Ile
NM_001173464.1:c.2841G>A NP_001166935.1:p.Met947Ile
NM_001173465.1:c.2733G>A NP_001166936.1:p.Met911Ile
NM_017641.3:c.2802G>A NP_060111.2:p.Met934Ile
XM_005269007.1:c.2841G>A XP_005269064.1:p.Met947Ile
XM_005269008.1:c.2841G>A XP_005269065.1:p.Met947Ile
XM_005269009.1:c.2841G>A XP_005269066.1:p.Met947Ile
XM_005269010.1:c.2802G>A XP_005269067.1:p.Met934Ile
XM_005269011.1:c.2841G>A XP_005269068.1:p.Met947Ile
XM_005269012.1:c.2841G>A XP_005269069.1:p.Met947Ile
XM_005269013.1:c.2841G>A XP_005269070.1:p.Met947Ile
XM_005269014.1:c.2841G>A XP_005269071.1:p.Met947Ile
XM_006719493.1:c.2802G>A XP_006719556.1:p.Met934Ile
XM_006719494.1:c.2841G>A XP_006719557.1:p.Met947Ile
XM_006719496.1:c.2802G>A XP_006719559.1:p.Met934Ile
XM_011538556.1:c.2772G>A XP_011536858.1:p.Met924Ile
XR_429108.1:n.3173G>A
XM_005269007.3:c.2841G>A XP_005269064.1:p.Met947Ile
XM_005269008.3:c.2841G>A XP_005269065.1:p.Met947Ile
XM_005269009.3:c.2841G>A XP_005269066.1:p.Met947Ile
XM_005269010.3:c.2802G>A XP_005269067.1:p.Met934Ile
XM_005269011.3:c.2841G>A XP_005269068.1:p.Met947Ile
XM_005269012.3:c.2841G>A XP_005269069.1:p.Met947Ile
XM_005269013.3:c.2841G>A XP_005269070.1:p.Met947Ile
XM_005269014.3:c.2841G>A XP_005269071.1:p.Met947Ile
XM_006719493.3:c.2802G>A XP_006719556.1:p.Met934Ile
XM_006719494.3:c.2841G>A XP_006719557.1:p.Met947Ile
XM_011538556.3:c.2772G>A XP_011536858.1:p.Met924Ile
XM_017019607.2:c.2802G>A XP_016875096.1:p.Met934Ile
XM_017019608.2:c.2802G>A XP_016875097.1:p.Met934Ile
XM_017019609.2:c.2802G>A XP_016875098.1:p.Met934Ile
XM_017019610.2:c.2841G>A XP_016875099.1:p.Met947Ile
XM_017019611.2:c.2802G>A XP_016875100.1:p.Met934Ile
NM_001173463.2:c.2802G>A NP_001166934.1:p.Met934Ile
NM_001173464.2:c.2841G>A MANE Select NP_001166935.1:p.Met947Ile
NM_001173465.2:c.2733G>A NP_001166936.1:p.Met911Ile
NM_017641.4:c.2802G>A NP_060111.2:p.Met934Ile
NM_001378439.1:c.2841G>A NP_001365368.1:p.Met947Ile
NM_001378440.1:c.2841G>A NP_001365369.1:p.Met947Ile
NM_001378441.1:c.2802G>A NP_001365370.1:p.Met934Ile