Canonical Allele Identifier: CA2194759753
Gene: KIF7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89631635G= , CM000677.2:g.89631635G= GRCh38
NC_000015.9:g.90174866G= , CM000677.1:g.90174866G= GRCh37
NC_000015.8:g.87975870G= NCBI36
NG_030338.1:g.28817C=

Transcript Alleles

HGVS Amino-acid change
ENST00000696512.1:c.3094C= ENSP00000512678.1:p.Gln1032=
ENST00000394412.8:c.2971C= MANE Select ENSP00000377934.3:p.Gln991=
ENST00000677187.1:n.645C=
ENST00000394412.7:c.2971C= ENSP00000377934.3:p.Gln991=
NM_198525.2:c.2971C= NP_940927.2:p.Gln991=
XM_005254902.2:c.2971C= XP_005254959.1:p.Gln991=
XM_011521531.1:c.3094C= XP_011519833.1:p.Gln1032=
XM_011521532.1:c.3091C= XP_011519834.1:p.Gln1031=
XM_011521533.1:c.3091C= XP_011519835.1:p.Gln1031=
XM_011521534.1:c.3094C= XP_011519836.1:p.Gln1032=
XM_011521535.1:c.3094C= XP_011519837.1:p.Gln1032=
XM_011521536.1:c.3094C= XP_011519838.1:p.Gln1032=
XM_011521531.2:c.3094C= XP_011519833.1:p.Gln1032=
NM_198525.3:c.2971C= MANE Select NP_940927.2:p.Gln991=