Canonical Allele Identifier: CA364350119
Gene: KIF6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.39357317C>A , CM000668.2:g.39357317C>A GRCh38
NC_000006.11:g.39325093C>A , CM000668.1:g.39325093C>A GRCh37
NC_000006.10:g.39433071C>A NCBI36
NG_054928.1:g.373108G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000287152.12:c.2140G>T MANE Select ENSP00000287152.7:p.Asp714Tyr
ENST00000229913.9:c.493G>T ENSP00000229913.5:p.Asp165Tyr
ENST00000287152.11:c.2140G>T ENSP00000287152.7:p.Asp714Tyr
ENST00000394362.5:c.493G>T ENSP00000377889.1:p.Asp165Tyr
ENST00000458470.5:c.1815G>T
ENST00000538893.5:c.493G>T ENSP00000441435.2:p.Asp165Tyr
NM_001289020.1:c.2089G>T NP_001275949.1:p.Asp697Tyr
NM_001289021.1:c.1972G>T NP_001275950.1:p.Asp658Tyr
NM_001289024.1:c.493G>T NP_001275953.1:p.Asp165Tyr
NM_145027.4:c.2140G>T NP_659464.3:p.Asp714Tyr
XM_005248904.3:c.2140G>T XP_005248961.1:p.Asp714Tyr
XM_011514357.1:c.2140G>T XP_011512659.1:p.Asp714Tyr
XM_011514358.1:c.2140G>T XP_011512660.1:p.Asp714Tyr
XM_011514359.1:c.2140G>T XP_011512661.1:p.Asp714Tyr
XM_011514360.1:c.1513G>T XP_011512662.1:p.Asp505Tyr
NM_001289020.2:c.2089G>T NP_001275949.1:p.Asp697Tyr
NM_001289021.2:c.1972G>T NP_001275950.1:p.Asp658Tyr
NM_001289024.2:c.493G>T NP_001275953.1:p.Asp165Tyr
NM_001351566.1:c.493G>T NP_001338495.1:p.Asp165Tyr
NM_145027.5:c.2140G>T NP_659464.3:p.Asp714Tyr
XM_005248904.4:c.2140G>T XP_005248961.1:p.Asp714Tyr
XM_011514357.3:c.2140G>T XP_011512659.1:p.Asp714Tyr
XM_011514358.3:c.2140G>T XP_011512660.1:p.Asp714Tyr
XM_011514359.3:c.2140G>T XP_011512661.1:p.Asp714Tyr
XM_017010427.1:c.1831G>T XP_016865916.1:p.Asp611Tyr
XM_017010428.1:c.1495G>T XP_016865917.1:p.Asp499Tyr
XR_001744111.1:n.75+5369C>A
NM_145027.6:c.2140G>T MANE Select NP_659464.3:p.Asp714Tyr
NM_001289020.3:c.2089G>T NP_001275949.1:p.Asp697Tyr
NM_001289021.3:c.1972G>T NP_001275950.1:p.Asp658Tyr
NM_001289024.3:c.493G>T NP_001275953.1:p.Asp165Tyr
NM_001351566.2:c.493G>T NP_001338495.1:p.Asp165Tyr