Canonical Allele Identifier: CA364350077
Gene: KIF6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.39357305C>G , CM000668.2:g.39357305C>G GRCh38
NC_000006.11:g.39325081C>G , CM000668.1:g.39325081C>G GRCh37
NC_000006.10:g.39433059C>G NCBI36
NG_054928.1:g.373120G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000287152.12:c.2152G>C MANE Select ENSP00000287152.7:p.Glu718Gln
ENST00000229913.9:c.505G>C ENSP00000229913.5:p.Glu169Gln
ENST00000287152.11:c.2152G>C ENSP00000287152.7:p.Glu718Gln
ENST00000394362.5:c.505G>C ENSP00000377889.1:p.Glu169Gln
ENST00000458470.5:c.1827G>C
ENST00000538893.5:c.505G>C ENSP00000441435.2:p.Glu169Gln
NM_001289020.1:c.2101G>C NP_001275949.1:p.Glu701Gln
NM_001289021.1:c.1984G>C NP_001275950.1:p.Glu662Gln
NM_001289024.1:c.505G>C NP_001275953.1:p.Glu169Gln
NM_145027.4:c.2152G>C NP_659464.3:p.Glu718Gln
XM_005248904.3:c.2152G>C XP_005248961.1:p.Glu718Gln
XM_011514357.1:c.2152G>C XP_011512659.1:p.Glu718Gln
XM_011514358.1:c.2152G>C XP_011512660.1:p.Glu718Gln
XM_011514359.1:c.2152G>C XP_011512661.1:p.Glu718Gln
XM_011514360.1:c.1525G>C XP_011512662.1:p.Glu509Gln
NM_001289020.2:c.2101G>C NP_001275949.1:p.Glu701Gln
NM_001289021.2:c.1984G>C NP_001275950.1:p.Glu662Gln
NM_001289024.2:c.505G>C NP_001275953.1:p.Glu169Gln
NM_001351566.1:c.505G>C NP_001338495.1:p.Glu169Gln
NM_145027.5:c.2152G>C NP_659464.3:p.Glu718Gln
XM_005248904.4:c.2152G>C XP_005248961.1:p.Glu718Gln
XM_011514357.3:c.2152G>C XP_011512659.1:p.Glu718Gln
XM_011514358.3:c.2152G>C XP_011512660.1:p.Glu718Gln
XM_011514359.3:c.2152G>C XP_011512661.1:p.Glu718Gln
XM_017010427.1:c.1843G>C XP_016865916.1:p.Glu615Gln
XM_017010428.1:c.1507G>C XP_016865917.1:p.Glu503Gln
XR_001744111.1:n.75+5357C>G
NM_145027.6:c.2152G>C MANE Select NP_659464.3:p.Glu718Gln
NM_001289020.3:c.2101G>C NP_001275949.1:p.Glu701Gln
NM_001289021.3:c.1984G>C NP_001275950.1:p.Glu662Gln
NM_001289024.3:c.505G>C NP_001275953.1:p.Glu169Gln
NM_001351566.2:c.505G>C NP_001338495.1:p.Glu169Gln