Canonical Allele Identifier: CA1622639576

Gene: KIF6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.39339107T= , CM000668.2:g.39339107T=	GRCh38
NC_000006.11:g.39306883T= , CM000668.1:g.39306883T=	GRCh37
NC_000006.10:g.39414861T=	NCBI36
NG_054928.1:g.391318A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287152.12:c.2429-2559A= MANE Select	ENSP00000287152.7:n.2429-2559A=
ENST00000229913.9:c.782-2559A=	ENSP00000229913.5:n.782-2559A=
ENST00000287152.11:c.2429-2559A=	ENSP00000287152.7:n.2429-2559A=
ENST00000394362.5:c.731-2559A=	ENSP00000377889.1:n.731-2559A=
ENST00000458470.5:c.2053-2559A=
NM_001289020.1:c.2378-2559A=	NP_001275949.1:n.2378-2559A=
NM_001289021.1:c.2261-2559A=	NP_001275950.1:n.2261-2559A=
NM_001289024.1:c.782-2559A=	NP_001275953.1:n.782-2559A=
NM_145027.4:c.2429-2559A=	NP_659464.3:n.2429-2559A=
XM_011514359.1:c.2378-2559A=	XP_011512661.1:n.2378-2559A=
XR_926774.1:n.238+429T=
NM_001289020.2:c.2378-2559A=	NP_001275949.1:n.2378-2559A=
NM_001289021.2:c.2261-2559A=	NP_001275950.1:n.2261-2559A=
NM_001289024.2:c.782-2559A=	NP_001275953.1:n.782-2559A=
NM_145027.5:c.2429-2559A=	NP_659464.3:n.2429-2559A=
XM_011514359.3:c.2378-2559A=	XP_011512661.1:n.2378-2559A=
XR_926774.2:n.248+429T=
NM_145027.6:c.2429-2559A= MANE Select	NP_659464.3:n.2429-2559A=
NM_001289020.3:c.2378-2559A=	NP_001275949.1:n.2378-2559A=
NM_001289021.3:c.2261-2559A=	NP_001275950.1:n.2261-2559A=
NM_001289024.3:c.782-2559A=	NP_001275953.1:n.782-2559A=