Linked Data
ClinVar Variation Id:
355144
ClinVar RCV Id:
RCV000347568
dbSNP Id:
rs886061001
gnomAD v3:
6-118559661-C-T
gnomAD v4:
6-118559661-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.118559661C>T , CM000668.2:g.118559661C>T | GRCh38 |
| NC_000006.11:g.118880824C>T , CM000668.1:g.118880824C>T | GRCh37 |
| NC_000006.10:g.118987517C>T | NCBI36 |
| NG_009082.1:g.16383C>T , LRG_390:g.16383C>T | |
| NG_021248.1:g.155415G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000357525.6:c.*581C>T (PLN) MANE Select | ENSP00000350132.5:n.*581C>T | |
| ENST00000368491.8:c.1020+5868G>A (CEP85L) MANE Select | ENSP00000357477.3:n.1020+5868G>A | |
| ENST00000357525.5:c.*581C>T (PLN) | ENSP00000350132.5:n.*581C>T | |
| ENST00000360290.7:c.714+5868G>A (CEP85L) | ENSP00000353434.3:n.714+5868G>A | |
| ENST00000368488.9:c.1029+5868G>A (CEP85L) | ENSP00000357474.5:n.1029+5868G>A | |
| ENST00000368491.7:c.1020+5868G>A (CEP85L) | ENSP00000357477.3:n.1020+5868G>A | |
| ENST00000392500.7:c.1029+5868G>A (CEP85L) | ENSP00000376288.3:n.1029+5868G>A | |
| ENST00000419517.2:c.1020+5868G>A (CEP85L) | ENSP00000393317.2:n.1020+5868G>A | |
| ENST00000434604.5:c.1029+5868G>A (CEP85L) | ENSP00000392131.1:n.1029+5868G>A | |
| NM_001042475.2:c.1020+5868G>A (CEP85L) | NP_001035940.1:n.1020+5868G>A | |
| NM_001178035.1:c.1029+5868G>A (CEP85L) | NP_001171506.1:n.1029+5868G>A | |
| NM_002667.3:c.*581C>T , LRG_390t1:c.*581C>T (PLN) | NP_002658.1:n.*581C>T | |
| NM_206921.2:c.1020+5868G>A (CEP85L) | NP_996804.2:n.1020+5868G>A | |
| XM_005266970.1:c.714+5868G>A (CEP85L) | XP_005267027.1:n.714+5868G>A | |
| XM_005266971.1:c.714+5868G>A (CEP85L) | XP_005267028.1:n.714+5868G>A | |
| XM_006715475.2:c.714+5868G>A (CEP85L) | XP_006715538.1:n.714+5868G>A | |
| XM_011535808.1:c.1029+5868G>A (CEP85L) | XP_011534110.1:n.1029+5868G>A | |
| XM_011535809.1:c.1020+5868G>A (CEP85L) | XP_011534111.1:n.1020+5868G>A | |
| XM_011535810.1:c.1029+5868G>A (CEP85L) | XP_011534112.1:n.1029+5868G>A | |
| XM_011535811.1:c.714+5868G>A (CEP85L) | XP_011534113.1:n.714+5868G>A | |
| XM_011535812.1:c.-67+4275G>A (CEP85L) | XP_011534114.1:n.-67+4275G>A | |
| NM_002667.4:c.*581C>T (PLN) | NP_002658.1:n.*581C>T | |
| XM_006715475.4:c.714+5868G>A (CEP85L) | XP_006715538.1:n.714+5868G>A | |
| XM_011535809.2:c.1020+5868G>A (CEP85L) | XP_011534111.1:n.1020+5868G>A | |
| XM_011535810.2:c.1029+5868G>A (CEP85L) | XP_011534112.1:n.1029+5868G>A | |
| XM_017010846.1:c.1029+5868G>A (CEP85L) | XP_016866335.1:n.1029+5868G>A | |
| XM_024446429.1:c.1020+5868G>A (CEP85L) | XP_024302197.1:n.1020+5868G>A | |
| XM_024446430.1:c.1020+5868G>A (CEP85L) | XP_024302198.1:n.1020+5868G>A | |
| NM_001042475.3:c.1020+5868G>A (CEP85L) MANE Select | NP_001035940.1:n.1020+5868G>A | |
| NM_002667.5:c.*581C>T (PLN) MANE Select | NP_002658.1:n.*581C>T | |
| NM_206921.3:c.1020+5868G>A (CEP85L) | NP_996804.2:n.1020+5868G>A | |
| NM_001178035.2:c.1029+5868G>A (CEP85L) | NP_001171506.1:n.1029+5868G>A |