Canonical Allele Identifier: CA450098186

Gene: KIF6

Linked Data

• MyVariant Identifiers: chr6:g.39325079T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.39357303T>C , CM000668.2:g.39357303T>C	GRCh38
NC_000006.11:g.39325079T>C , CM000668.1:g.39325079T>C	GRCh37
NC_000006.10:g.39433057T>C	NCBI36
NG_054928.1:g.373122A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000287152.12:c.2154A>G MANE Select	ENSP00000287152.7:p.Glu718=
ENST00000229913.9:c.507A>G	ENSP00000229913.5:p.Glu169=
ENST00000287152.11:c.2154A>G	ENSP00000287152.7:p.Glu718=
ENST00000394362.5:c.507A>G	ENSP00000377889.1:p.Glu169=
ENST00000458470.5:c.1829A>G
ENST00000538893.5:c.507A>G	ENSP00000441435.2:p.Glu169=
NM_001289020.1:c.2103A>G	NP_001275949.1:p.Glu701=
NM_001289021.1:c.1986A>G	NP_001275950.1:p.Glu662=
NM_001289024.1:c.507A>G	NP_001275953.1:p.Glu169=
NM_145027.4:c.2154A>G	NP_659464.3:p.Glu718=
XM_005248904.3:c.2154A>G	XP_005248961.1:p.Glu718=
XM_011514357.1:c.2154A>G	XP_011512659.1:p.Glu718=
XM_011514358.1:c.2154A>G	XP_011512660.1:p.Glu718=
XM_011514359.1:c.2154A>G	XP_011512661.1:p.Glu718=
XM_011514360.1:c.1527A>G	XP_011512662.1:p.Glu509=
NM_001289020.2:c.2103A>G	NP_001275949.1:p.Glu701=
NM_001289021.2:c.1986A>G	NP_001275950.1:p.Glu662=
NM_001289024.2:c.507A>G	NP_001275953.1:p.Glu169=
NM_001351566.1:c.507A>G	NP_001338495.1:p.Glu169=
NM_145027.5:c.2154A>G	NP_659464.3:p.Glu718=
XM_005248904.4:c.2154A>G	XP_005248961.1:p.Glu718=
XM_011514357.3:c.2154A>G	XP_011512659.1:p.Glu718=
XM_011514358.3:c.2154A>G	XP_011512660.1:p.Glu718=
XM_011514359.3:c.2154A>G	XP_011512661.1:p.Glu718=
XM_017010427.1:c.1845A>G	XP_016865916.1:p.Glu615=
XM_017010428.1:c.1509A>G	XP_016865917.1:p.Glu503=
XR_001744111.1:n.75+5355T>C
NM_145027.6:c.2154A>G MANE Select	NP_659464.3:p.Glu718=
NM_001289020.3:c.2103A>G	NP_001275949.1:p.Glu701=
NM_001289021.3:c.1986A>G	NP_001275950.1:p.Glu662=
NM_001289024.3:c.507A>G	NP_001275953.1:p.Glu169=
NM_001351566.2:c.507A>G	NP_001338495.1:p.Glu169=