Linked Data
dbSNP Id:
rs201317467
gnomAD v2:
22-32500704-G-GC
gnomAD v3:
22-32104717-G-GC
gnomAD v4:
22-32104717-G-GC
COSMIC:
COSN19662132
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.32104724dup , CM000684.2:g.32104724dup | GRCh38 |
| NC_000022.10:g.32500711dup , CM000684.1:g.32500711dup | GRCh37 |
| NC_000022.9:g.30830711dup | NCBI36 |
| NG_017045.1:g.66693dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266088.9:c.1666-62dup MANE Select | ENSP00000266088.4:n.1666-62dup | |
| ENST00000266088.8:c.1666-62dup | ENSP00000266088.4:n.1666-62dup | |
| ENST00000543737.2:c.1285-62dup | ENSP00000444898.1:n.1285-62dup | |
| NM_000343.3:c.1666-62dup | NP_000334.1:n.1666-62dup | |
| NM_001256314.1:c.1285-62dup | NP_001243243.1:n.1285-62dup | |
| XR_938173.1:n.591+2120dup | ||
| XR_938174.1:n.486+15137dup | ||
| NM_000343.4:c.1666-62dup MANE Select | NP_000334.1:n.1666-62dup | |
| NM_001256314.2:c.1285-62dup | NP_001243243.1:n.1285-62dup |