Canonical Allele Identifier: CA2194759535
Gene: KIF7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89631574C= , CM000677.2:g.89631574C= GRCh38
NC_000015.9:g.90174805C= , CM000677.1:g.90174805C= GRCh37
NC_000015.8:g.87975809C= NCBI36
NG_030338.1:g.28878G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000696512.1:c.3155G= ENSP00000512678.1:p.Arg1052=
ENST00000394412.8:c.3032G= MANE Select ENSP00000377934.3:p.Arg1011=
ENST00000677187.1:n.706G=
ENST00000394412.7:c.3032G= ENSP00000377934.3:p.Arg1011=
NM_198525.2:c.3032G= NP_940927.2:p.Arg1011=
XM_005254902.2:c.3032G= XP_005254959.1:p.Arg1011=
XM_011521531.1:c.3155G= XP_011519833.1:p.Arg1052=
XM_011521532.1:c.3152G= XP_011519834.1:p.Arg1051=
XM_011521533.1:c.3152G= XP_011519835.1:p.Arg1051=
XM_011521534.1:c.3155G= XP_011519836.1:p.Arg1052=
XM_011521535.1:c.3155G= XP_011519837.1:p.Arg1052=
XM_011521536.1:c.3155G= XP_011519838.1:p.Arg1052=
XM_011521531.2:c.3155G= XP_011519833.1:p.Arg1052=
NM_198525.3:c.3032G= MANE Select NP_940927.2:p.Arg1011=