Canonical Allele Identifier: CA3793807

Gene: KIF6

Linked Data

• dbSNP Id: rs372001923
• ExAC: 6:39325111 G / T
• gnomAD v4: 6-39357335-G-T
• MyVariant Identifiers: chr6:g.39325111G>T (hg19) ; chr6:g.39357335G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.39357335G>T , CM000668.2:g.39357335G>T	GRCh38
NC_000006.11:g.39325111G>T , CM000668.1:g.39325111G>T	GRCh37
NC_000006.10:g.39433089G>T	NCBI36
NG_054928.1:g.373090C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000287152.12:c.2122C>A MANE Select	ENSP00000287152.7:p.Pro708Thr
ENST00000229913.9:c.475C>A	ENSP00000229913.5:p.Pro159Thr
ENST00000287152.11:c.2122C>A	ENSP00000287152.7:p.Pro708Thr
ENST00000394362.5:c.475C>A	ENSP00000377889.1:p.Pro159Thr
ENST00000458470.5:c.1797C>A
ENST00000538893.5:c.475C>A	ENSP00000441435.2:p.Pro159Thr
NM_001289020.1:c.2071C>A	NP_001275949.1:p.Pro691Thr
NM_001289021.1:c.1954C>A	NP_001275950.1:p.Pro652Thr
NM_001289024.1:c.475C>A	NP_001275953.1:p.Pro159Thr
NM_145027.4:c.2122C>A	NP_659464.3:p.Pro708Thr
XM_005248904.3:c.2122C>A	XP_005248961.1:p.Pro708Thr
XM_011514357.1:c.2122C>A	XP_011512659.1:p.Pro708Thr
XM_011514358.1:c.2122C>A	XP_011512660.1:p.Pro708Thr
XM_011514359.1:c.2122C>A	XP_011512661.1:p.Pro708Thr
XM_011514360.1:c.1495C>A	XP_011512662.1:p.Pro499Thr
NM_001289020.2:c.2071C>A	NP_001275949.1:p.Pro691Thr
NM_001289021.2:c.1954C>A	NP_001275950.1:p.Pro652Thr
NM_001289024.2:c.475C>A	NP_001275953.1:p.Pro159Thr
NM_001351566.1:c.475C>A	NP_001338495.1:p.Pro159Thr
NM_145027.5:c.2122C>A	NP_659464.3:p.Pro708Thr
XM_005248904.4:c.2122C>A	XP_005248961.1:p.Pro708Thr
XM_011514357.3:c.2122C>A	XP_011512659.1:p.Pro708Thr
XM_011514358.3:c.2122C>A	XP_011512660.1:p.Pro708Thr
XM_011514359.3:c.2122C>A	XP_011512661.1:p.Pro708Thr
XM_017010427.1:c.1813C>A	XP_016865916.1:p.Pro605Thr
XM_017010428.1:c.1477C>A	XP_016865917.1:p.Pro493Thr
XR_001744111.1:n.75+5387G>T
NM_145027.6:c.2122C>A MANE Select	NP_659464.3:p.Pro708Thr
NM_001289020.3:c.2071C>A	NP_001275949.1:p.Pro691Thr
NM_001289021.3:c.1954C>A	NP_001275950.1:p.Pro652Thr
NM_001289024.3:c.475C>A	NP_001275953.1:p.Pro159Thr
NM_001351566.2:c.475C>A	NP_001338495.1:p.Pro159Thr