Canonical Allele Identifier: CA1622646665

Gene: KIF6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.39357184_39357185delinsTC , CM000668.2:g.39357184_39357185delinsTC	GRCh38
NC_000006.11:g.39324960_39324961delinsTC , CM000668.1:g.39324960_39324961delinsTC	GRCh37
NC_000006.10:g.39432938_39432939delinsTC	NCBI36
NG_054928.1:g.373240_373241delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287152.12:c.2180+92_2180+93delinsGA MANE Select	ENSP00000287152.7:n.2180+92_2180+93delinsGA
ENST00000229913.9:c.533+92_533+93delinsGA	ENSP00000229913.5:n.533+92_533+93delinsGA
ENST00000287152.11:c.2180+92_2180+93delinsGA	ENSP00000287152.7:n.2180+92_2180+93delinsGA
ENST00000394362.5:c.533+92_533+93delinsGA	ENSP00000377889.1:n.533+92_533+93delinsGA
ENST00000458470.5:c.1855+92_1855+93delinsGA
ENST00000538893.5:c.533+92_533+93delinsGA	ENSP00000441435.2:n.533+92_533+93delinsGA
NM_001289020.1:c.2129+92_2129+93delinsGA	NP_001275949.1:n.2129+92_2129+93delinsGA
NM_001289021.1:c.2012+92_2012+93delinsGA	NP_001275950.1:n.2012+92_2012+93delinsGA
NM_001289024.1:c.533+92_533+93delinsGA	NP_001275953.1:n.533+92_533+93delinsGA
NM_145027.4:c.2180+92_2180+93delinsGA	NP_659464.3:n.2180+92_2180+93delinsGA
XM_005248904.3:c.2180+92_2180+93delinsGA	XP_005248961.1:n.2180+92_2180+93delinsGA
XM_011514357.1:c.2180+92_2180+93delinsGA	XP_011512659.1:n.2180+92_2180+93delinsGA
XM_011514358.1:c.2180+92_2180+93delinsGA	XP_011512660.1:n.2180+92_2180+93delinsGA
XM_011514359.1:c.2180+92_2180+93delinsGA	XP_011512661.1:n.2180+92_2180+93delinsGA
XM_011514360.1:c.1553+92_1553+93delinsGA	XP_011512662.1:n.1553+92_1553+93delinsGA
NM_001289020.2:c.2129+92_2129+93delinsGA	NP_001275949.1:n.2129+92_2129+93delinsGA
NM_001289021.2:c.2012+92_2012+93delinsGA	NP_001275950.1:n.2012+92_2012+93delinsGA
NM_001289024.2:c.533+92_533+93delinsGA	NP_001275953.1:n.533+92_533+93delinsGA
NM_001351566.1:c.533+92_533+93delinsGA	NP_001338495.1:n.533+92_533+93delinsGA
NM_145027.5:c.2180+92_2180+93delinsGA	NP_659464.3:n.2180+92_2180+93delinsGA
XM_005248904.4:c.2180+92_2180+93delinsGA	XP_005248961.1:n.2180+92_2180+93delinsGA
XM_011514357.3:c.2180+92_2180+93delinsGA	XP_011512659.1:n.2180+92_2180+93delinsGA
XM_011514358.3:c.2180+92_2180+93delinsGA	XP_011512660.1:n.2180+92_2180+93delinsGA
XM_011514359.3:c.2180+92_2180+93delinsGA	XP_011512661.1:n.2180+92_2180+93delinsGA
XM_017010427.1:c.1871+92_1871+93delinsGA	XP_016865916.1:n.1871+92_1871+93delinsGA
XM_017010428.1:c.1535+92_1535+93delinsGA	XP_016865917.1:n.1535+92_1535+93delinsGA
XR_001744111.1:n.75+5236_75+5237delinsTC
NM_145027.6:c.2180+92_2180+93delinsGA MANE Select	NP_659464.3:n.2180+92_2180+93delinsGA
NM_001289020.3:c.2129+92_2129+93delinsGA	NP_001275949.1:n.2129+92_2129+93delinsGA
NM_001289021.3:c.2012+92_2012+93delinsGA	NP_001275950.1:n.2012+92_2012+93delinsGA
NM_001289024.3:c.533+92_533+93delinsGA	NP_001275953.1:n.533+92_533+93delinsGA
NM_001351566.2:c.533+92_533+93delinsGA	NP_001338495.1:n.533+92_533+93delinsGA