Canonical Allele Identifier: CA10646693
Gene: KIF7 HGNC NCBI

Linked Data

ClinVar Variation Id: 317372
ClinVar RCV Id: RCV000314210
dbSNP Id: rs886051538

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89648738C>T , CM000677.2:g.89648738C>T GRCh38
NC_000015.9:g.90191969C>T , CM000677.1:g.90191969C>T GRCh37
NC_000015.8:g.87992973C>T NCBI36
NG_030338.1:g.11714G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696512.1:c.1083G>A ENSP00000512678.1:p.Thr361=
ENST00000394412.8:c.960G>A MANE Select ENSP00000377934.3:p.Thr320=
ENST00000394412.7:c.960G>A ENSP00000377934.3:p.Thr320=
ENST00000445906.1:c.*619G>A ENSP00000395906.1:n.*619G>A
NM_198525.2:c.960G>A NP_940927.2:p.Thr320=
XM_005254902.2:c.960G>A XP_005254959.1:p.Thr320=
XM_011521531.1:c.1083G>A XP_011519833.1:p.Thr361=
XM_011521532.1:c.1083G>A XP_011519834.1:p.Thr361=
XM_011521533.1:c.1083G>A XP_011519835.1:p.Thr361=
XM_011521534.1:c.1083G>A XP_011519836.1:p.Thr361=
XM_011521535.1:c.1083G>A XP_011519837.1:p.Thr361=
XM_011521536.1:c.1083G>A XP_011519838.1:p.Thr361=
XM_011521537.1:c.1083G>A XP_011519839.1:p.Thr361=
XM_011521531.2:c.1083G>A XP_011519833.1:p.Thr361=
NM_198525.3:c.960G>A MANE Select NP_940927.2:p.Thr320=