Canonical Allele Identifier: CA364350163
Gene: KIF6 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000287152.12:c.2126T>C MANE Select ENSP00000287152.7:p.Phe709Ser
ENST00000229913.9:c.479T>C ENSP00000229913.5:p.Phe160Ser
ENST00000287152.11:c.2126T>C ENSP00000287152.7:p.Phe709Ser
ENST00000394362.5:c.479T>C ENSP00000377889.1:p.Phe160Ser
ENST00000458470.5:c.1801T>C
ENST00000538893.5:c.479T>C ENSP00000441435.2:p.Phe160Ser
NM_001289020.1:c.2075T>C NP_001275949.1:p.Phe692Ser
NM_001289021.1:c.1958T>C NP_001275950.1:p.Phe653Ser
NM_001289024.1:c.479T>C NP_001275953.1:p.Phe160Ser
NM_145027.4:c.2126T>C NP_659464.3:p.Phe709Ser
XM_005248904.3:c.2126T>C XP_005248961.1:p.Phe709Ser
XM_011514357.1:c.2126T>C XP_011512659.1:p.Phe709Ser
XM_011514358.1:c.2126T>C XP_011512660.1:p.Phe709Ser
XM_011514359.1:c.2126T>C XP_011512661.1:p.Phe709Ser
XM_011514360.1:c.1499T>C XP_011512662.1:p.Phe500Ser
NM_001289020.2:c.2075T>C NP_001275949.1:p.Phe692Ser
NM_001289021.2:c.1958T>C NP_001275950.1:p.Phe653Ser
NM_001289024.2:c.479T>C NP_001275953.1:p.Phe160Ser
NM_001351566.1:c.479T>C NP_001338495.1:p.Phe160Ser
NM_145027.5:c.2126T>C NP_659464.3:p.Phe709Ser
XM_005248904.4:c.2126T>C XP_005248961.1:p.Phe709Ser
XM_011514357.3:c.2126T>C XP_011512659.1:p.Phe709Ser
XM_011514358.3:c.2126T>C XP_011512660.1:p.Phe709Ser
XM_011514359.3:c.2126T>C XP_011512661.1:p.Phe709Ser
XM_017010427.1:c.1817T>C XP_016865916.1:p.Phe606Ser
XM_017010428.1:c.1481T>C XP_016865917.1:p.Phe494Ser
XR_001744111.1:n.75+5383A>G
NM_145027.6:c.2126T>C MANE Select NP_659464.3:p.Phe709Ser
NM_001289020.3:c.2075T>C NP_001275949.1:p.Phe692Ser
NM_001289021.3:c.1958T>C NP_001275950.1:p.Phe653Ser
NM_001289024.3:c.479T>C NP_001275953.1:p.Phe160Ser
NM_001351566.2:c.479T>C NP_001338495.1:p.Phe160Ser