Linked Data
ClinVar Variation Id:
2769109
ClinVar RCV Id:
RCV003578602
dbSNP Id:
rs1763575075
gnomAD v4:
6-43042922-G-A
MyVariant Identifiers:
chr6:g.43010660G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.43042922G>A , CM000668.2:g.43042922G>A | GRCh38 |
| NC_000006.11:g.43010660G>A , CM000668.1:g.43010660G>A | GRCh37 |
| NC_000006.10:g.43118638G>A | NCBI36 |
| NG_016205.1:g.16024C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000478630.2:n.1596C>T (CUL7) | ||
| ENST00000674112.2:c.3525C>T (CUL7) | ENSP00000501166.2:p.His1175= | |
| ENST00000685042.1:c.*181C>T (CUL7) | ENSP00000509871.1:n.*181C>T | |
| ENST00000686442.1:n.4086C>T (CUL7) | ||
| ENST00000687225.1:c.*1822C>T (CUL7) | ENSP00000509364.1:n.*1822C>T | |
| ENST00000688302.1:n.3808C>T (CUL7) | ||
| ENST00000689256.1:n.4102C>T (CUL7) | ||
| ENST00000690231.1:c.3525C>T (CUL7) | ENSP00000508461.1:p.His1175= | |
| ENST00000265348.9:c.3525C>T (CUL7) MANE Select | ENSP00000265348.4:p.His1175= | |
| ENST00000673725.1:c.1412-16C>T (CUL7) | ||
| ENST00000673753.1:n.4364C>T (CUL7) | ||
| ENST00000674100.1:c.3621C>T (CUL7) | ENSP00000501292.1:p.His1207= | |
| ENST00000674112.1:c.2017C>T (CUL7) | ||
| ENST00000674134.1:c.3621C>T (CUL7) | ENSP00000501068.1:p.His1207= | |
| ENST00000265348.7:c.3525C>T (CUL7) | ENSP00000265348.3:p.His1175= | |
| ENST00000467906.5:c.-1003-136G>A (KLC4) | ENSP00000418759.1:n.-1003-136G>A | |
| ENST00000535468.1:c.3777C>T (CUL7) | ENSP00000438788.1:p.His1259= | |
| NM_001168370.1:c.3777C>T (CUL7) | NP_001161842.1:p.His1259= | |
| NM_014780.4:c.3525C>T (CUL7) | NP_055595.2:p.His1175= | |
| XM_005249503.1:c.3681C>T (CUL7) | XP_005249560.1:p.His1227= | |
| XM_006715285.1:c.3621C>T (CUL7) | XP_006715348.1:p.His1207= | |
| XM_011515019.1:c.3777C>T (CUL7) | XP_011513321.1:p.His1259= | |
| XM_011515020.1:c.3681C>T (CUL7) | XP_011513322.1:p.His1227= | |
| XM_011515021.1:c.1386C>T (CUL7) | XP_011513323.1:p.His462= | |
| XM_005249503.3:c.3681C>T (CUL7) | XP_005249560.1:p.His1227= | |
| XM_006715285.2:c.3621C>T (CUL7) | XP_006715348.1:p.His1207= | |
| XM_011515019.2:c.3777C>T (CUL7) | XP_011513321.1:p.His1259= | |
| XM_011515020.2:c.3681C>T (CUL7) | XP_011513322.1:p.His1227= | |
| XM_017011533.1:c.3804C>T (CUL7) | XP_016867022.1:p.His1268= | |
| XM_017011534.1:c.3804C>T (CUL7) | XP_016867023.1:p.His1268= | |
| XM_017011535.1:c.3708C>T (CUL7) | XP_016867024.1:p.His1236= | |
| XM_017011536.2:c.3648C>T (CUL7) | XP_016867025.1:p.His1216= | |
| XM_017011537.2:c.3621C>T (CUL7) | XP_016867026.1:p.His1207= | |
| XM_017011538.2:c.3552C>T (CUL7) | XP_016867027.1:p.His1184= | |
| XM_017011539.2:c.3525C>T (CUL7) | XP_016867028.1:p.His1175= | |
| NM_001168370.2:c.3621C>T (CUL7) | NP_001161842.2:p.His1207= | |
| NM_001374872.1:c.3621C>T (CUL7) | NP_001361801.1:p.His1207= | |
| NM_001374873.1:c.3525C>T (CUL7) | NP_001361802.1:p.His1175= | |
| NM_001374874.1:c.3522C>T (CUL7) | NP_001361803.1:p.His1174= | |
| NM_014780.5:c.3525C>T (CUL7) MANE Select | NP_055595.2:p.His1175= |