Canonical Allele Identifier: CA137716028

Gene: KIF6

Linked Data

• dbSNP Id: rs9462535
• gnomAD v3: 6-39348016-C-T
• gnomAD v4: 6-39348016-C-T
• MyVariant Identifiers: chr6:g.39315792C>T (hg19) ; chr6:g.39348016C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.39348016C>T , CM000668.2:g.39348016C>T	GRCh38
NC_000006.11:g.39315792C>T , CM000668.1:g.39315792C>T	GRCh37
NC_000006.10:g.39423770C>T	NCBI36
NG_054928.1:g.382409G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000287152.12:c.2181-1490G>A MANE Select	ENSP00000287152.7:n.2181-1490G>A
ENST00000229913.9:c.534-1490G>A	ENSP00000229913.5:n.534-1490G>A
ENST00000287152.11:c.2181-1490G>A	ENSP00000287152.7:n.2181-1490G>A
ENST00000394362.5:c.534-2227G>A	ENSP00000377889.1:n.534-2227G>A
ENST00000458470.5:c.1856-2227G>A
ENST00000538893.5:c.534-1490G>A	ENSP00000441435.2:n.534-1490G>A
NM_001289020.1:c.2130-1490G>A	NP_001275949.1:n.2130-1490G>A
NM_001289021.1:c.2013-1490G>A	NP_001275950.1:n.2013-1490G>A
NM_001289024.1:c.534-1490G>A	NP_001275953.1:n.534-1490G>A
NM_145027.4:c.2181-1490G>A	NP_659464.3:n.2181-1490G>A
XM_005248904.3:c.2181-1490G>A	XP_005248961.1:n.2181-1490G>A
XM_011514357.1:c.2181-2227G>A	XP_011512659.1:n.2181-2227G>A
XM_011514358.1:c.2181-1490G>A	XP_011512660.1:n.2181-1490G>A
XM_011514359.1:c.2181-2227G>A	XP_011512661.1:n.2181-2227G>A
XM_011514360.1:c.1554-1490G>A	XP_011512662.1:n.1554-1490G>A
NM_001289020.2:c.2130-1490G>A	NP_001275949.1:n.2130-1490G>A
NM_001289021.2:c.2013-1490G>A	NP_001275950.1:n.2013-1490G>A
NM_001289024.2:c.534-1490G>A	NP_001275953.1:n.534-1490G>A
NM_001351566.1:c.534-1490G>A	NP_001338495.1:n.534-1490G>A
NM_145027.5:c.2181-1490G>A	NP_659464.3:n.2181-1490G>A
XM_005248904.4:c.2181-1490G>A	XP_005248961.1:n.2181-1490G>A
XM_011514357.3:c.2181-2227G>A	XP_011512659.1:n.2181-2227G>A
XM_011514358.3:c.2181-1490G>A	XP_011512660.1:n.2181-1490G>A
XM_011514359.3:c.2181-2227G>A	XP_011512661.1:n.2181-2227G>A
XM_017010427.1:c.1872-1490G>A	XP_016865916.1:n.1872-1490G>A
XM_017010428.1:c.1536-1490G>A	XP_016865917.1:n.1536-1490G>A
NM_145027.6:c.2181-1490G>A MANE Select	NP_659464.3:n.2181-1490G>A
NM_001289020.3:c.2130-1490G>A	NP_001275949.1:n.2130-1490G>A
NM_001289021.3:c.2013-1490G>A	NP_001275950.1:n.2013-1490G>A
NM_001289024.3:c.534-1490G>A	NP_001275953.1:n.534-1490G>A
NM_001351566.2:c.534-1490G>A	NP_001338495.1:n.534-1490G>A