Canonical Allele Identifier: CA020289

Gene: KIF7

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89633187C>G , CM000677.2:g.89633187C>G	GRCh38
NC_000015.9:g.90176418C>G , CM000677.1:g.90176418C>G	GRCh37
NC_000015.8:g.87977422C>G	NCBI36
NG_030338.1:g.27265G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696512.1:c.2795G>C	ENSP00000512678.1:p.Arg932Thr
ENST00000394412.8:c.2672G>C MANE Select	ENSP00000377934.3:p.Arg891Thr
ENST00000677187.1:n.346G>C
ENST00000394412.7:c.2672G>C	ENSP00000377934.3:p.Arg891Thr
NM_198525.2:c.2672G>C	NP_940927.2:p.Arg891Thr
XM_005254902.2:c.2672G>C	XP_005254959.1:p.Arg891Thr
XM_011521531.1:c.2795G>C	XP_011519833.1:p.Arg932Thr
XM_011521532.1:c.2792G>C	XP_011519834.1:p.Arg931Thr
XM_011521533.1:c.2792G>C	XP_011519835.1:p.Arg931Thr
XM_011521534.1:c.2795G>C	XP_011519836.1:p.Arg932Thr
XM_011521535.1:c.2795G>C	XP_011519837.1:p.Arg932Thr
XM_011521536.1:c.2795G>C	XP_011519838.1:p.Arg932Thr
XM_011521537.1:c.*67G>C	XP_011519839.1:n.*67G>C
XM_011521531.2:c.2795G>C	XP_011519833.1:p.Arg932Thr
NM_198525.3:c.2672G>C MANE Select	NP_940927.2:p.Arg891Thr