Canonical Allele Identifier: CA2194759223

Gene: KIF7

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89631427G= , CM000677.2:g.89631427G=	GRCh38
NC_000015.9:g.90174658G= , CM000677.1:g.90174658G=	GRCh37
NC_000015.8:g.87975662G=	NCBI36
NG_030338.1:g.29025C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696512.1:c.3234+68C=	ENSP00000512678.1:n.3234+68C=
ENST00000394412.8:c.3111+68C= MANE Select	ENSP00000377934.3:n.3111+68C=
ENST00000677187.1:n.785+68C=
ENST00000394412.7:c.3111+68C=	ENSP00000377934.3:n.3111+68C=
NM_198525.2:c.3111+68C=	NP_940927.2:n.3111+68C=
XM_005254902.2:c.3111+68C=	XP_005254959.1:n.3111+68C=
XM_011521531.1:c.3234+68C=	XP_011519833.1:n.3234+68C=
XM_011521532.1:c.3231+68C=	XP_011519834.1:n.3231+68C=
XM_011521533.1:c.3231+68C=	XP_011519835.1:n.3231+68C=
XM_011521534.1:c.3234+68C=	XP_011519836.1:n.3234+68C=
XM_011521535.1:c.3234+68C=	XP_011519837.1:n.3234+68C=
XM_011521536.1:c.3234+68C=	XP_011519838.1:n.3234+68C=
XM_011521531.2:c.3234+68C=	XP_011519833.1:n.3234+68C=
NM_198525.3:c.3111+68C= MANE Select	NP_940927.2:n.3111+68C=