Canonical Allele Identifier: CA2843446756

Gene: KIF7

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89631616del , CM000677.2:g.89631616del	GRCh38
NC_000015.9:g.90174847del , CM000677.1:g.90174847del	GRCh37
NC_000015.8:g.87975851del	NCBI36
NG_030338.1:g.28838del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696512.1:c.3115del	ENSP00000512678.1:p.Gln1039ArgfsTer?
ENST00000394412.8:c.2992del MANE Select	ENSP00000377934.3:p.Gln998ArgfsTer?
ENST00000677187.1:n.666del
ENST00000394412.7:c.2992del	ENSP00000377934.3:p.Gln998ArgfsTer?
NM_198525.2:c.2992del	NP_940927.2:p.Gln998ArgfsTer?
XM_005254902.2:c.2992del	XP_005254959.1:p.Gln998ArgfsTer?
XM_011521531.1:c.3115del	XP_011519833.1:p.Gln1039ArgfsTer?
XM_011521532.1:c.3112del	XP_011519834.1:p.Gln1038ArgfsTer?
XM_011521533.1:c.3112del	XP_011519835.1:p.Gln1038ArgfsTer?
XM_011521534.1:c.3115del	XP_011519836.1:p.Gln1039ArgfsTer?
XM_011521535.1:c.3115del	XP_011519837.1:p.Gln1039ArgfsTer?
XM_011521536.1:c.3115del	XP_011519838.1:p.Gln1039ArgfsTer?
XM_011521531.2:c.3115del	XP_011519833.1:p.Gln1039ArgfsTer?
NM_198525.3:c.2992del MANE Select	NP_940927.2:p.Gln998ArgfsTer?