Linked Data
ClinVar Variation Id:
317349
ClinVar RCV Id:
RCV000404350
dbSNP Id:
rs886051529
gnomAD v3:
15-89628494-C-A
gnomAD v4:
15-89628494-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.89628494C>A , CM000677.2:g.89628494C>A | GRCh38 |
| NC_000015.9:g.90171725C>A , CM000677.1:g.90171725C>A | GRCh37 |
| NC_000015.8:g.87972729C>A | NCBI36 |
| NG_030338.1:g.31958G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696512.1:c.4080G>T (KIF7) | ENSP00000512678.1:p.Gly1360= | |
| ENST00000394412.8:c.3957G>T (KIF7) MANE Select | ENSP00000377934.3:p.Gly1319= | |
| ENST00000677187.1:n.1631G>T (KIF7) | ||
| ENST00000394412.7:c.3957G>T (KIF7) | ENSP00000377934.3:p.Gly1319= | |
| ENST00000558928.1:n.180+107G>T (KIF7) | ||
| ENST00000561095.1:c.741-936C>A (TICRR) | ||
| NM_198525.2:c.3957G>T (KIF7) | NP_940927.2:p.Gly1319= | |
| XM_005254902.2:c.3957G>T (KIF7) | XP_005254959.1:p.Gly1319= | |
| XM_011521531.1:c.4080G>T (KIF7) | XP_011519833.1:p.Gly1360= | |
| XM_011521532.1:c.4077G>T (KIF7) | XP_011519834.1:p.Gly1359= | |
| XM_011521533.1:c.4077G>T (KIF7) | XP_011519835.1:p.Gly1359= | |
| XM_011521534.1:c.3973+107G>T (KIF7) | XP_011519836.1:n.3973+107G>T | |
| XM_011521535.1:c.3973+107G>T (KIF7) | XP_011519837.1:n.3973+107G>T | |
| XM_011521536.1:c.3973+107G>T (KIF7) | XP_011519838.1:n.3973+107G>T | |
| XM_011521531.2:c.4080G>T (KIF7) | XP_011519833.1:p.Gly1360= | |
| NM_198525.3:c.3957G>T (KIF7) MANE Select | NP_940927.2:p.Gly1319= |