Canonical Allele Identifier: CA1622646830

Gene: KIF6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.39357339C= , CM000668.2:g.39357339C=	GRCh38
NC_000006.11:g.39325115C= , CM000668.1:g.39325115C=	GRCh37
NC_000006.10:g.39433093C=	NCBI36
NG_054928.1:g.373086G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000287152.12:c.2118G= MANE Select	ENSP00000287152.7:p.Thr706=
ENST00000229913.9:c.471G=	ENSP00000229913.5:p.Thr157=
ENST00000287152.11:c.2118G=	ENSP00000287152.7:p.Thr706=
ENST00000394362.5:c.471G=	ENSP00000377889.1:p.Thr157=
ENST00000458470.5:c.1793G=
ENST00000538893.5:c.471G=	ENSP00000441435.2:p.Thr157=
NM_001289020.1:c.2067G=	NP_001275949.1:p.Thr689=
NM_001289021.1:c.1950G=	NP_001275950.1:p.Thr650=
NM_001289024.1:c.471G=	NP_001275953.1:p.Thr157=
NM_145027.4:c.2118G=	NP_659464.3:p.Thr706=
XM_005248904.3:c.2118G=	XP_005248961.1:p.Thr706=
XM_011514357.1:c.2118G=	XP_011512659.1:p.Thr706=
XM_011514358.1:c.2118G=	XP_011512660.1:p.Thr706=
XM_011514359.1:c.2118G=	XP_011512661.1:p.Thr706=
XM_011514360.1:c.1491G=	XP_011512662.1:p.Thr497=
NM_001289020.2:c.2067G=	NP_001275949.1:p.Thr689=
NM_001289021.2:c.1950G=	NP_001275950.1:p.Thr650=
NM_001289024.2:c.471G=	NP_001275953.1:p.Thr157=
NM_001351566.1:c.471G=	NP_001338495.1:p.Thr157=
NM_145027.5:c.2118G=	NP_659464.3:p.Thr706=
XM_005248904.4:c.2118G=	XP_005248961.1:p.Thr706=
XM_011514357.3:c.2118G=	XP_011512659.1:p.Thr706=
XM_011514358.3:c.2118G=	XP_011512660.1:p.Thr706=
XM_011514359.3:c.2118G=	XP_011512661.1:p.Thr706=
XM_017010427.1:c.1809G=	XP_016865916.1:p.Thr603=
XM_017010428.1:c.1473G=	XP_016865917.1:p.Thr491=
XR_001744111.1:n.75+5391C=
NM_145027.6:c.2118G= MANE Select	NP_659464.3:p.Thr706=
NM_001289020.3:c.2067G=	NP_001275949.1:p.Thr689=
NM_001289021.3:c.1950G=	NP_001275950.1:p.Thr650=
NM_001289024.3:c.471G=	NP_001275953.1:p.Thr157=
NM_001351566.2:c.471G=	NP_001338495.1:p.Thr157=