Canonical Allele Identifier: CA450098201

Gene: KIF6

Linked Data

• MyVariant Identifiers: chr6:g.39325106A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.39357330A>G , CM000668.2:g.39357330A>G	GRCh38
NC_000006.11:g.39325106A>G , CM000668.1:g.39325106A>G	GRCh37
NC_000006.10:g.39433084A>G	NCBI36
NG_054928.1:g.373095T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000287152.12:c.2127T>C MANE Select	ENSP00000287152.7:p.Phe709=
ENST00000229913.9:c.480T>C	ENSP00000229913.5:p.Phe160=
ENST00000287152.11:c.2127T>C	ENSP00000287152.7:p.Phe709=
ENST00000394362.5:c.480T>C	ENSP00000377889.1:p.Phe160=
ENST00000458470.5:c.1802T>C
ENST00000538893.5:c.480T>C	ENSP00000441435.2:p.Phe160=
NM_001289020.1:c.2076T>C	NP_001275949.1:p.Phe692=
NM_001289021.1:c.1959T>C	NP_001275950.1:p.Phe653=
NM_001289024.1:c.480T>C	NP_001275953.1:p.Phe160=
NM_145027.4:c.2127T>C	NP_659464.3:p.Phe709=
XM_005248904.3:c.2127T>C	XP_005248961.1:p.Phe709=
XM_011514357.1:c.2127T>C	XP_011512659.1:p.Phe709=
XM_011514358.1:c.2127T>C	XP_011512660.1:p.Phe709=
XM_011514359.1:c.2127T>C	XP_011512661.1:p.Phe709=
XM_011514360.1:c.1500T>C	XP_011512662.1:p.Phe500=
NM_001289020.2:c.2076T>C	NP_001275949.1:p.Phe692=
NM_001289021.2:c.1959T>C	NP_001275950.1:p.Phe653=
NM_001289024.2:c.480T>C	NP_001275953.1:p.Phe160=
NM_001351566.1:c.480T>C	NP_001338495.1:p.Phe160=
NM_145027.5:c.2127T>C	NP_659464.3:p.Phe709=
XM_005248904.4:c.2127T>C	XP_005248961.1:p.Phe709=
XM_011514357.3:c.2127T>C	XP_011512659.1:p.Phe709=
XM_011514358.3:c.2127T>C	XP_011512660.1:p.Phe709=
XM_011514359.3:c.2127T>C	XP_011512661.1:p.Phe709=
XM_017010427.1:c.1818T>C	XP_016865916.1:p.Phe606=
XM_017010428.1:c.1482T>C	XP_016865917.1:p.Phe494=
XR_001744111.1:n.75+5382A>G
NM_145027.6:c.2127T>C MANE Select	NP_659464.3:p.Phe709=
NM_001289020.3:c.2076T>C	NP_001275949.1:p.Phe692=
NM_001289021.3:c.1959T>C	NP_001275950.1:p.Phe653=
NM_001289024.3:c.480T>C	NP_001275953.1:p.Phe160=
NM_001351566.2:c.480T>C	NP_001338495.1:p.Phe160=