Canonical Allele Identifier: CA1622646798
Gene: KIF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.39357302A= , CM000668.2:g.39357302A= GRCh38
NC_000006.11:g.39325078A= , CM000668.1:g.39325078A= GRCh37
NC_000006.10:g.39433056A= NCBI36
NG_054928.1:g.373123T=

Transcript Alleles

HGVS Amino-acid change
ENST00000287152.12:c.2155T= MANE Select ENSP00000287152.7:p.Trp719=
ENST00000229913.9:c.508T= ENSP00000229913.5:p.Trp170=
ENST00000287152.11:c.2155T= ENSP00000287152.7:p.Trp719=
ENST00000394362.5:c.508T= ENSP00000377889.1:p.Trp170=
ENST00000458470.5:c.1830T=
ENST00000538893.5:c.508T= ENSP00000441435.2:p.Trp170=
NM_001289020.1:c.2104T= NP_001275949.1:p.Trp702=
NM_001289021.1:c.1987T= NP_001275950.1:p.Trp663=
NM_001289024.1:c.508T= NP_001275953.1:p.Trp170=
NM_145027.4:c.2155T= NP_659464.3:p.Trp719=
XM_005248904.3:c.2155T= XP_005248961.1:p.Trp719=
XM_011514357.1:c.2155T= XP_011512659.1:p.Trp719=
XM_011514358.1:c.2155T= XP_011512660.1:p.Trp719=
XM_011514359.1:c.2155T= XP_011512661.1:p.Trp719=
XM_011514360.1:c.1528T= XP_011512662.1:p.Trp510=
NM_001289020.2:c.2104T= NP_001275949.1:p.Trp702=
NM_001289021.2:c.1987T= NP_001275950.1:p.Trp663=
NM_001289024.2:c.508T= NP_001275953.1:p.Trp170=
NM_001351566.1:c.508T= NP_001338495.1:p.Trp170=
NM_145027.5:c.2155T= NP_659464.3:p.Trp719=
XM_005248904.4:c.2155T= XP_005248961.1:p.Trp719=
XM_011514357.3:c.2155T= XP_011512659.1:p.Trp719=
XM_011514358.3:c.2155T= XP_011512660.1:p.Trp719=
XM_011514359.3:c.2155T= XP_011512661.1:p.Trp719=
XM_017010427.1:c.1846T= XP_016865916.1:p.Trp616=
XM_017010428.1:c.1510T= XP_016865917.1:p.Trp504=
XR_001744111.1:n.75+5354A=
NM_145027.6:c.2155T= MANE Select NP_659464.3:p.Trp719=
NM_001289020.3:c.2104T= NP_001275949.1:p.Trp702=
NM_001289021.3:c.1987T= NP_001275950.1:p.Trp663=
NM_001289024.3:c.508T= NP_001275953.1:p.Trp170=
NM_001351566.2:c.508T= NP_001338495.1:p.Trp170=