Canonical Allele Identifier: CA1088128671

Gene: KIF6

Linked Data

• gnomAD v3: 6-39357063-TGG-T
• gnomAD v4: 6-39357063-TGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.39357064_39357065del , CM000668.2:g.39357064_39357065del	GRCh38
NC_000006.11:g.39324840_39324841del , CM000668.1:g.39324840_39324841del	GRCh37
NC_000006.10:g.39432818_39432819del	NCBI36
NG_054928.1:g.373360_373361del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287152.12:c.2180+212_2180+213del MANE Select	ENSP00000287152.7:n.2180+212_2180+213del
ENST00000229913.9:c.533+212_533+213del	ENSP00000229913.5:n.533+212_533+213del
ENST00000287152.11:c.2180+212_2180+213del	ENSP00000287152.7:n.2180+212_2180+213del
ENST00000394362.5:c.533+212_533+213del	ENSP00000377889.1:n.533+212_533+213del
ENST00000458470.5:c.1855+212_1855+213del
ENST00000538893.5:c.533+212_533+213del	ENSP00000441435.2:n.533+212_533+213del
NM_001289020.1:c.2129+212_2129+213del	NP_001275949.1:n.2129+212_2129+213del
NM_001289021.1:c.2012+212_2012+213del	NP_001275950.1:n.2012+212_2012+213del
NM_001289024.1:c.533+212_533+213del	NP_001275953.1:n.533+212_533+213del
NM_145027.4:c.2180+212_2180+213del	NP_659464.3:n.2180+212_2180+213del
XM_005248904.3:c.2180+212_2180+213del	XP_005248961.1:n.2180+212_2180+213del
XM_011514357.1:c.2180+212_2180+213del	XP_011512659.1:n.2180+212_2180+213del
XM_011514358.1:c.2180+212_2180+213del	XP_011512660.1:n.2180+212_2180+213del
XM_011514359.1:c.2180+212_2180+213del	XP_011512661.1:n.2180+212_2180+213del
XM_011514360.1:c.1553+212_1553+213del	XP_011512662.1:n.1553+212_1553+213del
NM_001289020.2:c.2129+212_2129+213del	NP_001275949.1:n.2129+212_2129+213del
NM_001289021.2:c.2012+212_2012+213del	NP_001275950.1:n.2012+212_2012+213del
NM_001289024.2:c.533+212_533+213del	NP_001275953.1:n.533+212_533+213del
NM_001351566.1:c.533+212_533+213del	NP_001338495.1:n.533+212_533+213del
NM_145027.5:c.2180+212_2180+213del	NP_659464.3:n.2180+212_2180+213del
XM_005248904.4:c.2180+212_2180+213del	XP_005248961.1:n.2180+212_2180+213del
XM_011514357.3:c.2180+212_2180+213del	XP_011512659.1:n.2180+212_2180+213del
XM_011514358.3:c.2180+212_2180+213del	XP_011512660.1:n.2180+212_2180+213del
XM_011514359.3:c.2180+212_2180+213del	XP_011512661.1:n.2180+212_2180+213del
XM_017010427.1:c.1871+212_1871+213del	XP_016865916.1:n.1871+212_1871+213del
XM_017010428.1:c.1535+212_1535+213del	XP_016865917.1:n.1535+212_1535+213del
XR_001744111.1:n.75+5116_75+5117del
NM_145027.6:c.2180+212_2180+213del MANE Select	NP_659464.3:n.2180+212_2180+213del
NM_001289020.3:c.2129+212_2129+213del	NP_001275949.1:n.2129+212_2129+213del
NM_001289021.3:c.2012+212_2012+213del	NP_001275950.1:n.2012+212_2012+213del
NM_001289024.3:c.533+212_533+213del	NP_001275953.1:n.533+212_533+213del
NM_001351566.2:c.533+212_533+213del	NP_001338495.1:n.533+212_533+213del