Canonical Allele Identifier: CA364350074
Gene: KIF6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.39357304T>G , CM000668.2:g.39357304T>G GRCh38
NC_000006.11:g.39325080T>G , CM000668.1:g.39325080T>G GRCh37
NC_000006.10:g.39433058T>G NCBI36
NG_054928.1:g.373121A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000287152.12:c.2153A>C MANE Select ENSP00000287152.7:p.Glu718Ala
ENST00000229913.9:c.506A>C ENSP00000229913.5:p.Glu169Ala
ENST00000287152.11:c.2153A>C ENSP00000287152.7:p.Glu718Ala
ENST00000394362.5:c.506A>C ENSP00000377889.1:p.Glu169Ala
ENST00000458470.5:c.1828A>C
ENST00000538893.5:c.506A>C ENSP00000441435.2:p.Glu169Ala
NM_001289020.1:c.2102A>C NP_001275949.1:p.Glu701Ala
NM_001289021.1:c.1985A>C NP_001275950.1:p.Glu662Ala
NM_001289024.1:c.506A>C NP_001275953.1:p.Glu169Ala
NM_145027.4:c.2153A>C NP_659464.3:p.Glu718Ala
XM_005248904.3:c.2153A>C XP_005248961.1:p.Glu718Ala
XM_011514357.1:c.2153A>C XP_011512659.1:p.Glu718Ala
XM_011514358.1:c.2153A>C XP_011512660.1:p.Glu718Ala
XM_011514359.1:c.2153A>C XP_011512661.1:p.Glu718Ala
XM_011514360.1:c.1526A>C XP_011512662.1:p.Glu509Ala
NM_001289020.2:c.2102A>C NP_001275949.1:p.Glu701Ala
NM_001289021.2:c.1985A>C NP_001275950.1:p.Glu662Ala
NM_001289024.2:c.506A>C NP_001275953.1:p.Glu169Ala
NM_001351566.1:c.506A>C NP_001338495.1:p.Glu169Ala
NM_145027.5:c.2153A>C NP_659464.3:p.Glu718Ala
XM_005248904.4:c.2153A>C XP_005248961.1:p.Glu718Ala
XM_011514357.3:c.2153A>C XP_011512659.1:p.Glu718Ala
XM_011514358.3:c.2153A>C XP_011512660.1:p.Glu718Ala
XM_011514359.3:c.2153A>C XP_011512661.1:p.Glu718Ala
XM_017010427.1:c.1844A>C XP_016865916.1:p.Glu615Ala
XM_017010428.1:c.1508A>C XP_016865917.1:p.Glu503Ala
XR_001744111.1:n.75+5356T>G
NM_145027.6:c.2153A>C MANE Select NP_659464.3:p.Glu718Ala
NM_001289020.3:c.2102A>C NP_001275949.1:p.Glu701Ala
NM_001289021.3:c.1985A>C NP_001275950.1:p.Glu662Ala
NM_001289024.3:c.506A>C NP_001275953.1:p.Glu169Ala
NM_001351566.2:c.506A>C NP_001338495.1:p.Glu169Ala