Canonical Allele Identifier: CA2194759489

Gene: KIF7

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89631536_89631545delinsTCTCCAGGCG , CM000677.2:g.89631536_89631545delinsTCTCCAGGCG	GRCh38
NC_000015.9:g.90174767_90174776delinsTCTCCAGGCG , CM000677.1:g.90174767_90174776delinsTCTCCAGGCG	GRCh37
NC_000015.8:g.87975771_87975780delinsTCTCCAGGCG	NCBI36
NG_030338.1:g.28907_28916delinsCGCCTGGAGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000696512.1:c.3184_3193delinsCGCCTGGAGA	ENSP00000512678.1:p.Arg1062=
ENST00000394412.8:c.3061_3070delinsCGCCTGGAGA MANE Select	ENSP00000377934.3:p.Arg1021=
ENST00000677187.1:n.735_744delinsCGCCTGGAGA
ENST00000394412.7:c.3061_3070delinsCGCCTGGAGA	ENSP00000377934.3:p.Arg1021=
NM_198525.2:c.3061_3070delinsCGCCTGGAGA	NP_940927.2:p.Arg1021=
XM_005254902.2:c.3061_3070delinsCGCCTGGAGA	XP_005254959.1:p.Arg1021=
XM_011521531.1:c.3184_3193delinsCGCCTGGAGA	XP_011519833.1:p.Arg1062=
XM_011521532.1:c.3181_3190delinsCGCCTGGAGA	XP_011519834.1:p.Arg1061=
XM_011521533.1:c.3181_3190delinsCGCCTGGAGA	XP_011519835.1:p.Arg1061=
XM_011521534.1:c.3184_3193delinsCGCCTGGAGA	XP_011519836.1:p.Arg1062=
XM_011521535.1:c.3184_3193delinsCGCCTGGAGA	XP_011519837.1:p.Arg1062=
XM_011521536.1:c.3184_3193delinsCGCCTGGAGA	XP_011519838.1:p.Arg1062=
XM_011521531.2:c.3184_3193delinsCGCCTGGAGA	XP_011519833.1:p.Arg1062=
NM_198525.3:c.3061_3070delinsCGCCTGGAGA MANE Select	NP_940927.2:p.Arg1021=