Canonical Allele Identifier: CA450098208

Gene: KIF6

Linked Data

• MyVariant Identifiers: chr6:g.39325118G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.39357342G>A , CM000668.2:g.39357342G>A	GRCh38
NC_000006.11:g.39325118G>A , CM000668.1:g.39325118G>A	GRCh37
NC_000006.10:g.39433096G>A	NCBI36
NG_054928.1:g.373083C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000287152.12:c.2115C>T MANE Select	ENSP00000287152.7:p.His705=
ENST00000229913.9:c.468C>T	ENSP00000229913.5:p.His156=
ENST00000287152.11:c.2115C>T	ENSP00000287152.7:p.His705=
ENST00000394362.5:c.468C>T	ENSP00000377889.1:p.His156=
ENST00000458470.5:c.1790C>T
ENST00000538893.5:c.468C>T	ENSP00000441435.2:p.His156=
NM_001289020.1:c.2064C>T	NP_001275949.1:p.His688=
NM_001289021.1:c.1947C>T	NP_001275950.1:p.His649=
NM_001289024.1:c.468C>T	NP_001275953.1:p.His156=
NM_145027.4:c.2115C>T	NP_659464.3:p.His705=
XM_005248904.3:c.2115C>T	XP_005248961.1:p.His705=
XM_011514357.1:c.2115C>T	XP_011512659.1:p.His705=
XM_011514358.1:c.2115C>T	XP_011512660.1:p.His705=
XM_011514359.1:c.2115C>T	XP_011512661.1:p.His705=
XM_011514360.1:c.1488C>T	XP_011512662.1:p.His496=
NM_001289020.2:c.2064C>T	NP_001275949.1:p.His688=
NM_001289021.2:c.1947C>T	NP_001275950.1:p.His649=
NM_001289024.2:c.468C>T	NP_001275953.1:p.His156=
NM_001351566.1:c.468C>T	NP_001338495.1:p.His156=
NM_145027.5:c.2115C>T	NP_659464.3:p.His705=
XM_005248904.4:c.2115C>T	XP_005248961.1:p.His705=
XM_011514357.3:c.2115C>T	XP_011512659.1:p.His705=
XM_011514358.3:c.2115C>T	XP_011512660.1:p.His705=
XM_011514359.3:c.2115C>T	XP_011512661.1:p.His705=
XM_017010427.1:c.1806C>T	XP_016865916.1:p.His602=
XM_017010428.1:c.1470C>T	XP_016865917.1:p.His490=
XR_001744111.1:n.75+5394G>A
NM_145027.6:c.2115C>T MANE Select	NP_659464.3:p.His705=
NM_001289020.3:c.2064C>T	NP_001275949.1:p.His688=
NM_001289021.3:c.1947C>T	NP_001275950.1:p.His649=
NM_001289024.3:c.468C>T	NP_001275953.1:p.His156=
NM_001351566.2:c.468C>T	NP_001338495.1:p.His156=