Canonical Allele Identifier: CA2194760028

Gene: KIF7

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89631725A= , CM000677.2:g.89631725A=	GRCh38
NC_000015.9:g.90174956A= , CM000677.1:g.90174956A=	GRCh37
NC_000015.8:g.87975960A=	NCBI36
NG_030338.1:g.28727T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696512.1:c.3019-15T=	ENSP00000512678.1:n.3019-15T=
ENST00000394412.8:c.2896-15T= MANE Select	ENSP00000377934.3:n.2896-15T=
ENST00000677187.1:n.570-15T=
ENST00000394412.7:c.2896-15T=	ENSP00000377934.3:n.2896-15T=
NM_198525.2:c.2896-15T=	NP_940927.2:n.2896-15T=
XM_005254902.2:c.2896-15T=	XP_005254959.1:n.2896-15T=
XM_011521531.1:c.3019-15T=	XP_011519833.1:n.3019-15T=
XM_011521532.1:c.3016-15T=	XP_011519834.1:n.3016-15T=
XM_011521533.1:c.3016-15T=	XP_011519835.1:n.3016-15T=
XM_011521534.1:c.3019-15T=	XP_011519836.1:n.3019-15T=
XM_011521535.1:c.3019-15T=	XP_011519837.1:n.3019-15T=
XM_011521536.1:c.3019-15T=	XP_011519838.1:n.3019-15T=
XM_011521531.2:c.3019-15T=	XP_011519833.1:n.3019-15T=
NM_198525.3:c.2896-15T= MANE Select	NP_940927.2:n.2896-15T=