Linked Data
ClinVar Variation Id:
3078967
ClinVar RCV Id:
RCV004375256
dbSNP Id:
rs1003781109
gnomAD v2:
6-43018830-G-A
gnomAD v3:
6-43051092-G-A
gnomAD v4:
6-43051092-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.43051092G>A , CM000668.2:g.43051092G>A | GRCh38 |
| NC_000006.11:g.43018830G>A , CM000668.1:g.43018830G>A | GRCh37 |
| NC_000006.10:g.43126808G>A | NCBI36 |
| NG_016205.1:g.7854C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000674112.2:c.1109C>T (CUL7) | ENSP00000501166.2:p.Ala370Val | |
| ENST00000683160.1:n.1491C>T (CUL7) | ||
| ENST00000683493.1:n.1150C>T (CUL7) | ||
| ENST00000685042.1:c.1109C>T (CUL7) | ENSP00000509871.1:p.Ala370Val | |
| ENST00000686442.1:n.1392C>T (CUL7) | ||
| ENST00000687225.1:c.1205C>T (CUL7) | ENSP00000509364.1:p.Ala402Val | |
| ENST00000688302.1:n.1392C>T (CUL7) | ||
| ENST00000688707.1:c.1205C>T (CUL7) | ENSP00000510608.1:p.Ala402Val | |
| ENST00000689256.1:n.1408C>T (CUL7) | ||
| ENST00000690231.1:c.1109C>T (CUL7) | ENSP00000508461.1:p.Ala370Val | |
| ENST00000265348.9:c.1109C>T (CUL7) MANE Select | ENSP00000265348.4:p.Ala370Val | |
| ENST00000673753.1:n.1443C>T (CUL7) | ||
| ENST00000673761.1:c.1860C>T | ENSP00000501018.1:n.1860C>T | |
| ENST00000674100.1:c.1205C>T (CUL7) | ENSP00000501292.1:p.Ala402Val | |
| ENST00000674134.1:c.1205C>T (CUL7) | ENSP00000501068.1:p.Ala402Val | |
| ENST00000265348.7:c.1109C>T (CUL7) | ENSP00000265348.3:p.Ala370Val | |
| ENST00000467906.5:c.-553+7584G>A (KLC4) | ENSP00000418759.1:n.-553+7584G>A | |
| ENST00000535468.1:c.1361C>T (CUL7) | ENSP00000438788.1:p.Ala454Val | |
| NM_001168370.1:c.1361C>T (CUL7) | NP_001161842.1:p.Ala454Val | |
| NM_014780.4:c.1109C>T (CUL7) | NP_055595.2:p.Ala370Val | |
| XM_005249503.1:c.1265C>T (CUL7) | XP_005249560.1:p.Ala422Val | |
| XM_006715285.1:c.1205C>T (CUL7) | XP_006715348.1:p.Ala402Val | |
| XM_011515019.1:c.1361C>T (CUL7) | XP_011513321.1:p.Ala454Val | |
| XM_011515020.1:c.1265C>T (CUL7) | XP_011513322.1:p.Ala422Val | |
| XM_005249503.3:c.1265C>T (CUL7) | XP_005249560.1:p.Ala422Val | |
| XM_006715285.2:c.1205C>T (CUL7) | XP_006715348.1:p.Ala402Val | |
| XM_011515019.2:c.1361C>T (CUL7) | XP_011513321.1:p.Ala454Val | |
| XM_011515020.2:c.1265C>T (CUL7) | XP_011513322.1:p.Ala422Val | |
| XM_017011533.1:c.1361C>T (CUL7) | XP_016867022.1:p.Ala454Val | |
| XM_017011534.1:c.1361C>T (CUL7) | XP_016867023.1:p.Ala454Val | |
| XM_017011535.1:c.1265C>T (CUL7) | XP_016867024.1:p.Ala422Val | |
| XM_017011536.2:c.1205C>T (CUL7) | XP_016867025.1:p.Ala402Val | |
| XM_017011537.2:c.1205C>T (CUL7) | XP_016867026.1:p.Ala402Val | |
| XM_017011538.2:c.1109C>T (CUL7) | XP_016867027.1:p.Ala370Val | |
| XM_017011539.2:c.1109C>T (CUL7) | XP_016867028.1:p.Ala370Val | |
| XM_017011540.1:c.1361C>T (CUL7) | XP_016867029.1:p.Ala454Val | |
| NM_001168370.2:c.1205C>T (CUL7) | NP_001161842.2:p.Ala402Val | |
| NM_001374872.1:c.1205C>T (CUL7) | NP_001361801.1:p.Ala402Val | |
| NM_001374873.1:c.1109C>T (CUL7) | NP_001361802.1:p.Ala370Val | |
| NM_001374874.1:c.1109C>T (CUL7) | NP_001361803.1:p.Ala370Val | |
| NM_014780.5:c.1109C>T (CUL7) MANE Select | NP_055595.2:p.Ala370Val |