SUSPENSION NOTICE:2024-08-07T19:00:00-0500 — 2024-10-16T08:00:00-0500
New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
This migration is underway but taking longer than originally estimated.
New user registrations, changes to existing user profiles, and changes to user credentials will be suspended for several weeks.
This allows us to avoid multi-day, broad service outages as we continue to migrate off our current cloud hosting provider.
This migration is underway but taking longer than originally estimated.
Linked Data
ClinVar Variation Id:
252305
ClinVar RCV Id:
RCV000238328
dbSNP Id:
rs879255190
PubMed:
PMID:15199436
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11128089dup , CM000681.2:g.11128089dup | GRCh38 |
| NC_000019.9:g.11238765dup , CM000681.1:g.11238765dup | GRCh37 |
| NC_000019.8:g.11099765dup | NCBI36 |
| NG_009060.1:g.43709dup , LRG_274:g.43709dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252444.10:c.2647+4dup | ENSP00000252444.6:n.2647+4dup | |
| ENST00000559340.2:c.*458+4dup | ENSP00000453696.2:n.*458+4dup | |
| ENST00000560467.2:c.2269+4dup | ENSP00000453513.2:n.2269+4dup | |
| ENST00000558518.6:c.2389+4dup MANE Select | ENSP00000454071.1:n.2389+4dup | |
| ENST00000252444.9:c.2643+4dup | ||
| ENST00000455727.6:c.1885+4dup | ENSP00000397829.2:n.1885+4dup | |
| ENST00000535915.5:c.2266+4dup | ENSP00000440520.1:n.2266+4dup | |
| ENST00000545707.5:c.1855+4dup | ENSP00000437639.1:n.1855+4dup | |
| ENST00000557933.5:c.2389+4dup | ENSP00000453557.1:n.2389+4dup | |
| ENST00000558013.5:c.2389+4dup | ENSP00000453346.1:n.2389+4dup | |
| ENST00000558518.5:c.2389+4dup | ENSP00000454071.1:n.2389+4dup | |
| ENST00000560628.1:n.108+435dup | ||
| NM_000527.4:c.2389+4dup , LRG_274t1:c.2389+4dup | NP_000518.1:n.2389+4dup | |
| NM_001195798.1:c.2389+4dup | NP_001182727.1:n.2389+4dup | |
| NM_001195799.1:c.2266+4dup | NP_001182728.1:n.2266+4dup | |
| NM_001195800.1:c.1885+4dup | NP_001182729.1:n.1885+4dup | |
| NM_001195803.1:c.1855+4dup | NP_001182732.1:n.1855+4dup | |
| XM_011528010.1:c.2312-1424dup | XP_011526312.1:n.2312-1424dup | |
| XM_011528011.1:c.2008+4dup | XP_011526313.1:n.2008+4dup | |
| XR_244074.2:n.2399+4dup | ||
| XM_011528010.2:c.2312-1424dup | XP_011526312.1:n.2312-1424dup | |
| XR_001753685.2:n.2723+4dup | ||
| XR_001753686.2:n.2366+4dup | ||
| NM_000527.5:c.2389+4dup MANE Select | NP_000518.1:n.2389+4dup | |
| NM_001195798.2:c.2389+4dup | NP_001182727.1:n.2389+4dup | |
| NM_001195799.2:c.2266+4dup | NP_001182728.1:n.2266+4dup | |
| NM_001195800.2:c.1885+4dup | NP_001182729.1:n.1885+4dup | |
| NM_001195803.2:c.1855+4dup | NP_001182732.1:n.1855+4dup |