Canonical Allele Identifier: CA020341
Gene: KIF7 HGNC NCBI

Linked Data

ClinVar Variation Id: 96655
dbSNP Id: rs9672286

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89631558C>T , CM000677.2:g.89631558C>T GRCh38
NC_000015.9:g.90174789C>T , CM000677.1:g.90174789C>T GRCh37
NC_000015.8:g.87975793C>T NCBI36
NG_030338.1:g.28894G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000696512.1:c.3171G>A ENSP00000512678.1:p.Ser1057=
ENST00000394412.8:c.3048G>A MANE Select ENSP00000377934.3:p.Ser1016=
ENST00000677187.1:n.722G>A
ENST00000394412.7:c.3048G>A ENSP00000377934.3:p.Ser1016=
NM_198525.2:c.3048G>A NP_940927.2:p.Ser1016=
XM_005254902.2:c.3048G>A XP_005254959.1:p.Ser1016=
XM_011521531.1:c.3171G>A XP_011519833.1:p.Ser1057=
XM_011521532.1:c.3168G>A XP_011519834.1:p.Ser1056=
XM_011521533.1:c.3168G>A XP_011519835.1:p.Ser1056=
XM_011521534.1:c.3171G>A XP_011519836.1:p.Ser1057=
XM_011521535.1:c.3171G>A XP_011519837.1:p.Ser1057=
XM_011521536.1:c.3171G>A XP_011519838.1:p.Ser1057=
XM_011521531.2:c.3171G>A XP_011519833.1:p.Ser1057=
NM_198525.3:c.3048G>A MANE Select NP_940927.2:p.Ser1016=