Linked Data
ClinVar Variation Id:
332984
ClinVar RCV Id:
RCV000348470
dbSNP Id:
rs16867441
ExAC:
2:182401867 G / A
gnomAD v2:
2-182401867-G-A
gnomAD v3:
2-181537140-G-A
gnomAD v4:
2-181537140-G-A
COSMIC:
COSN5490732
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.181537140G>A , CM000664.2:g.181537140G>A | GRCh38 |
| NC_000002.11:g.182401867G>A , CM000664.1:g.182401867G>A | GRCh37 |
| NC_000002.10:g.182110112G>A | NCBI36 |
| NG_021178.1:g.124968C>T | |
| NG_050623.1:g.85249G>A | |
| NG_021178.2:g.124968C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684145.1:c.*1044C>T (CERKL) | ENSP00000508396.1:n.*1044C>T | |
| ENST00000397033.7:c.*1613G>A (ITGA4) MANE Select | ENSP00000380227.2:n.*1613G>A | |
| ENST00000410087.8:c.*1044C>T (CERKL) MANE Select | ENSP00000386725.3:n.*1044C>T | |
| ENST00000410087.7:c.*1044C>T (CERKL) | ENSP00000386725.3:n.*1044C>T | |
| NM_000885.4:c.*1613G>A (ITGA4) | NP_000876.3:n.*1613G>A | |
| NM_000885.5:c.*1613G>A (ITGA4) | NP_000876.3:n.*1613G>A | |
| NM_001030311.2:c.*1044C>T (CERKL) | NP_001025482.1:n.*1044C>T | |
| NM_001030312.2:c.*1044C>T (CERKL) | NP_001025483.1:n.*1044C>T | |
| NM_001030313.2:c.*1044C>T (CERKL) | NP_001025484.1:n.*1044C>T | |
| NM_001160277.1:c.*1044C>T (CERKL) | NP_001153749.1:n.*1044C>T | |
| NM_201548.4:c.*1044C>T (CERKL) | NP_963842.1:n.*1044C>T | |
| NR_027689.1:n.2548C>T (CERKL) | ||
| NR_027690.1:n.2680C>T (CERKL) | ||
| NM_000885.6:c.*1613G>A (ITGA4) MANE Select | NP_000876.3:n.*1613G>A | |
| NM_201548.5:c.*1044C>T (CERKL) MANE Select | NP_963842.1:n.*1044C>T | |
| NM_001030311.3:c.*1044C>T (CERKL) | NP_001025482.1:n.*1044C>T | |
| NM_001030312.3:c.*1044C>T (CERKL) | NP_001025483.1:n.*1044C>T | |
| NM_001030313.3:c.*1044C>T (CERKL) | NP_001025484.1:n.*1044C>T | |
| NM_001160277.2:c.*1044C>T (CERKL) | NP_001153749.1:n.*1044C>T | |
| NR_027689.2:n.2546C>T (CERKL) | ||
| NR_027690.2:n.2678C>T (CERKL) |