Linked Data
dbSNP Id:
rs10462028
gnomAD v2:
4-56298300-G-A
gnomAD v3:
4-55432133-G-A
gnomAD v4:
4-55432133-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.55432133G>A , CM000666.2:g.55432133G>A | GRCh38 |
| NC_000004.11:g.56298300G>A , CM000666.1:g.56298300G>A | GRCh37 |
| NC_000004.10:g.55993057G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000513440.6:c.*3282C>T (CLOCK) MANE Select | ENSP00000426983.1:n.*3282C>T | |
| ENST00000309964.8:c.*3282C>T (CLOCK) | ENSP00000308741.4:n.*3282C>T | |
| ENST00000506103.2:c.352+7490G>A (TMEM165) | ||
| ENST00000608091.1:c.408+7490G>A (TMEM165) | ||
| NM_001267843.1:c.*3282C>T (CLOCK) | NP_001254772.1:n.*3282C>T | |
| NM_004898.3:c.*3282C>T (CLOCK) | NP_004889.1:n.*3282C>T | |
| XM_005265787.1:c.*3282C>T (CLOCK) | XP_005265844.1:n.*3282C>T | |
| XM_006714054.2:c.*3282C>T (CLOCK) | XP_006714117.1:n.*3282C>T | |
| XM_011534394.1:c.898+7490G>A (TMEM165) | XP_011532696.1:n.898+7490G>A | |
| XM_011534409.1:c.*3282C>T (CLOCK) | XP_011532711.1:n.*3282C>T | |
| XM_011534410.1:c.*3282C>T (CLOCK) | XP_011532712.1:n.*3282C>T | |
| XM_011534411.1:c.*3282C>T (CLOCK) | XP_011532713.1:n.*3282C>T | |
| XM_005265787.2:c.*3282C>T (CLOCK) | XP_005265844.1:n.*3282C>T | |
| XM_011534394.3:c.898+7490G>A (TMEM165) | XP_011532696.1:n.898+7490G>A | |
| XM_011534409.2:c.*3282C>T (CLOCK) | XP_011532711.1:n.*3282C>T | |
| XM_011534410.2:c.*3282C>T (CLOCK) | XP_011532712.1:n.*3282C>T | |
| XM_011534411.2:c.*3282C>T (CLOCK) | XP_011532713.1:n.*3282C>T | |
| XM_017008854.1:c.*3282C>T (CLOCK) | XP_016864343.1:n.*3282C>T | |
| XM_017008855.1:c.*3282C>T (CLOCK) | XP_016864344.1:n.*3282C>T | |
| XM_024454284.1:c.*3282C>T (CLOCK) | XP_024310052.1:n.*3282C>T | |
| NM_004898.4:c.*3282C>T (CLOCK) MANE Select | NP_004889.1:n.*3282C>T | |
| NM_001267843.2:c.*3282C>T (CLOCK) | NP_001254772.1:n.*3282C>T |