Canonical Allele Identifier: CA364350130
Gene: KIF6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.39357322G>C , CM000668.2:g.39357322G>C GRCh38
NC_000006.11:g.39325098G>C , CM000668.1:g.39325098G>C GRCh37
NC_000006.10:g.39433076G>C NCBI36
NG_054928.1:g.373103C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000287152.12:c.2135C>G MANE Select ENSP00000287152.7:p.Thr712Arg
ENST00000229913.9:c.488C>G ENSP00000229913.5:p.Thr163Arg
ENST00000287152.11:c.2135C>G ENSP00000287152.7:p.Thr712Arg
ENST00000394362.5:c.488C>G ENSP00000377889.1:p.Thr163Arg
ENST00000458470.5:c.1810C>G
ENST00000538893.5:c.488C>G ENSP00000441435.2:p.Thr163Arg
NM_001289020.1:c.2084C>G NP_001275949.1:p.Thr695Arg
NM_001289021.1:c.1967C>G NP_001275950.1:p.Thr656Arg
NM_001289024.1:c.488C>G NP_001275953.1:p.Thr163Arg
NM_145027.4:c.2135C>G NP_659464.3:p.Thr712Arg
XM_005248904.3:c.2135C>G XP_005248961.1:p.Thr712Arg
XM_011514357.1:c.2135C>G XP_011512659.1:p.Thr712Arg
XM_011514358.1:c.2135C>G XP_011512660.1:p.Thr712Arg
XM_011514359.1:c.2135C>G XP_011512661.1:p.Thr712Arg
XM_011514360.1:c.1508C>G XP_011512662.1:p.Thr503Arg
NM_001289020.2:c.2084C>G NP_001275949.1:p.Thr695Arg
NM_001289021.2:c.1967C>G NP_001275950.1:p.Thr656Arg
NM_001289024.2:c.488C>G NP_001275953.1:p.Thr163Arg
NM_001351566.1:c.488C>G NP_001338495.1:p.Thr163Arg
NM_145027.5:c.2135C>G NP_659464.3:p.Thr712Arg
XM_005248904.4:c.2135C>G XP_005248961.1:p.Thr712Arg
XM_011514357.3:c.2135C>G XP_011512659.1:p.Thr712Arg
XM_011514358.3:c.2135C>G XP_011512660.1:p.Thr712Arg
XM_011514359.3:c.2135C>G XP_011512661.1:p.Thr712Arg
XM_017010427.1:c.1826C>G XP_016865916.1:p.Thr609Arg
XM_017010428.1:c.1490C>G XP_016865917.1:p.Thr497Arg
XR_001744111.1:n.75+5374G>C
NM_145027.6:c.2135C>G MANE Select NP_659464.3:p.Thr712Arg
NM_001289020.3:c.2084C>G NP_001275949.1:p.Thr695Arg
NM_001289021.3:c.1967C>G NP_001275950.1:p.Thr656Arg
NM_001289024.3:c.488C>G NP_001275953.1:p.Thr163Arg
NM_001351566.2:c.488C>G NP_001338495.1:p.Thr163Arg