Canonical Allele Identifier: CA137738153

Gene: KIF6

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.39561206G>A , CM000668.2:g.39561206G>A	GRCh38
NC_000006.11:g.39528982G>A , CM000668.1:g.39528982G>A	GRCh37
NC_000006.10:g.39636960G>A	NCBI36
NG_054928.1:g.169219C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287152.12:c.1182-15518C>T MANE Select	ENSP00000287152.7:n.1182-15518C>T
ENST00000287152.11:c.1182-15518C>T	ENSP00000287152.7:n.1182-15518C>T
ENST00000458470.5:c.857-15518C>T
ENST00000538893.5:c.-298-15518C>T	ENSP00000441435.2:n.-298-15518C>T
NM_001289020.1:c.1182-15518C>T	NP_001275949.1:n.1182-15518C>T
NM_001289021.1:c.1182-15518C>T	NP_001275950.1:n.1182-15518C>T
NM_145027.4:c.1182-15518C>T	NP_659464.3:n.1182-15518C>T
XM_005248904.3:c.1182-15518C>T	XP_005248961.1:n.1182-15518C>T
XM_011514357.1:c.1182-15518C>T	XP_011512659.1:n.1182-15518C>T
XM_011514358.1:c.1182-15518C>T	XP_011512660.1:n.1182-15518C>T
XM_011514359.1:c.1182-15518C>T	XP_011512661.1:n.1182-15518C>T
XM_011514360.1:c.555-15518C>T	XP_011512662.1:n.555-15518C>T
XM_011514361.1:c.1182-2781C>T	XP_011512663.1:n.1182-2781C>T
NM_001289020.2:c.1182-15518C>T	NP_001275949.1:n.1182-15518C>T
NM_001289021.2:c.1182-15518C>T	NP_001275950.1:n.1182-15518C>T
NM_145027.5:c.1182-15518C>T	NP_659464.3:n.1182-15518C>T
XM_005248904.4:c.1182-15518C>T	XP_005248961.1:n.1182-15518C>T
XM_011514357.3:c.1182-15518C>T	XP_011512659.1:n.1182-15518C>T
XM_011514358.3:c.1182-15518C>T	XP_011512660.1:n.1182-15518C>T
XM_011514359.3:c.1182-15518C>T	XP_011512661.1:n.1182-15518C>T
XM_011514361.2:c.1182-2781C>T	XP_011512663.1:n.1182-2781C>T
XM_017010427.1:c.873-15518C>T	XP_016865916.1:n.873-15518C>T
XM_017010428.1:c.537-15518C>T	XP_016865917.1:n.537-15518C>T
XR_001743238.1:n.1277-15518C>T
NM_145027.6:c.1182-15518C>T MANE Select	NP_659464.3:n.1182-15518C>T
NM_001289020.3:c.1182-15518C>T	NP_001275949.1:n.1182-15518C>T
NM_001289021.3:c.1182-15518C>T	NP_001275950.1:n.1182-15518C>T