Canonical Allele Identifier: CA364350161
Gene: KIF6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.39357331A>T , CM000668.2:g.39357331A>T GRCh38
NC_000006.11:g.39325107A>T , CM000668.1:g.39325107A>T GRCh37
NC_000006.10:g.39433085A>T NCBI36
NG_054928.1:g.373094T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000287152.12:c.2126T>A MANE Select ENSP00000287152.7:p.Phe709Tyr
ENST00000229913.9:c.479T>A ENSP00000229913.5:p.Phe160Tyr
ENST00000287152.11:c.2126T>A ENSP00000287152.7:p.Phe709Tyr
ENST00000394362.5:c.479T>A ENSP00000377889.1:p.Phe160Tyr
ENST00000458470.5:c.1801T>A
ENST00000538893.5:c.479T>A ENSP00000441435.2:p.Phe160Tyr
NM_001289020.1:c.2075T>A NP_001275949.1:p.Phe692Tyr
NM_001289021.1:c.1958T>A NP_001275950.1:p.Phe653Tyr
NM_001289024.1:c.479T>A NP_001275953.1:p.Phe160Tyr
NM_145027.4:c.2126T>A NP_659464.3:p.Phe709Tyr
XM_005248904.3:c.2126T>A XP_005248961.1:p.Phe709Tyr
XM_011514357.1:c.2126T>A XP_011512659.1:p.Phe709Tyr
XM_011514358.1:c.2126T>A XP_011512660.1:p.Phe709Tyr
XM_011514359.1:c.2126T>A XP_011512661.1:p.Phe709Tyr
XM_011514360.1:c.1499T>A XP_011512662.1:p.Phe500Tyr
NM_001289020.2:c.2075T>A NP_001275949.1:p.Phe692Tyr
NM_001289021.2:c.1958T>A NP_001275950.1:p.Phe653Tyr
NM_001289024.2:c.479T>A NP_001275953.1:p.Phe160Tyr
NM_001351566.1:c.479T>A NP_001338495.1:p.Phe160Tyr
NM_145027.5:c.2126T>A NP_659464.3:p.Phe709Tyr
XM_005248904.4:c.2126T>A XP_005248961.1:p.Phe709Tyr
XM_011514357.3:c.2126T>A XP_011512659.1:p.Phe709Tyr
XM_011514358.3:c.2126T>A XP_011512660.1:p.Phe709Tyr
XM_011514359.3:c.2126T>A XP_011512661.1:p.Phe709Tyr
XM_017010427.1:c.1817T>A XP_016865916.1:p.Phe606Tyr
XM_017010428.1:c.1481T>A XP_016865917.1:p.Phe494Tyr
XR_001744111.1:n.75+5383A>T
NM_145027.6:c.2126T>A MANE Select NP_659464.3:p.Phe709Tyr
NM_001289020.3:c.2075T>A NP_001275949.1:p.Phe692Tyr
NM_001289021.3:c.1958T>A NP_001275950.1:p.Phe653Tyr
NM_001289024.3:c.479T>A NP_001275953.1:p.Phe160Tyr
NM_001351566.2:c.479T>A NP_001338495.1:p.Phe160Tyr