Canonical Allele Identifier: CA2499225685
Gene: KIF16B HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.16312356_16312357del , CM000682.2:g.16312356_16312357del GRCh38
NC_000020.10:g.16293001_16293002del , CM000682.1:g.16293001_16293002del GRCh37
NC_000020.9:g.16241001_16241002del NCBI36
NG_028043.1:g.266078_266079del
NG_028043.2:g.266078_266079del

Transcript Alleles

HGVS Amino-acid Change
ENST00000354981.7:c.3773_3774del MANE Select ENSP00000347076.2:p.Ala1258GlyfsTer?
ENST00000636835.1:c.3620_3621del ENSP00000489838.1:p.Ala1207GlyfsTer?
ENST00000354981.6:c.3773_3774del ENSP00000347076.2:p.Ala1258GlyfsTer?
ENST00000355755.7:c.425_426del ENSP00000347995.4:p.Ala142GlyfsTer?
NM_001199865.1:c.3620_3621del NP_001186794.1:p.Ala1207GlyfsTer?
NM_024704.4:c.3773_3774del NP_078980.3:p.Ala1258GlyfsTer?
XM_005260753.2:c.3806_3807del XP_005260810.1:p.Ala1269GlyfsTer?
XM_005260754.2:c.3716_3717del XP_005260811.1:p.Ala1239GlyfsTer?
XM_005260755.2:c.3653_3654del XP_005260812.1:p.Ala1218GlyfsTer?
XM_006723588.2:c.3683_3684del XP_006723651.1:p.Ala1228GlyfsTer?
XM_005260753.3:c.3806_3807del XP_005260810.1:p.Ala1269GlyfsTer?
XM_005260754.3:c.3716_3717del XP_005260811.1:p.Ala1239GlyfsTer?
XM_005260755.3:c.3653_3654del XP_005260812.1:p.Ala1218GlyfsTer?
XM_006723588.3:c.3683_3684del XP_006723651.1:p.Ala1228GlyfsTer?
XM_017027926.1:c.3650_3651del XP_016883415.1:p.Ala1217GlyfsTer?
NM_001199865.2:c.3620_3621del NP_001186794.1:p.Ala1207GlyfsTer?
NM_024704.5:c.3773_3774del MANE Select NP_078980.3:p.Ala1258GlyfsTer?