Linked Data
gnomAD v4:
1-215779823-C-CTT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215779831_215779832dup , CM000663.2:g.215779831_215779832dup | GRCh38 |
| NC_000001.10:g.215953173_215953174dup , CM000663.1:g.215953173_215953174dup | GRCh37 |
| NC_000001.9:g.214019796_214019797dup | NCBI36 |
| NG_009497.1:g.648572_648573dup | |
| NG_009497.2:g.648624_648625dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.10939+18_10939+19dup MANE Select | ENSP00000305941.3:n.10939+18_10939+19dup | |
| ENST00000674083.1:c.10939+18_10939+19dup | ENSP00000501296.1:n.10939+18_10939+19dup | |
| ENST00000307340.7:c.10939+18_10939+19dup | ENSP00000305941.3:n.10939+18_10939+19dup | |
| NM_206933.2:c.10939+18_10939+19dup | NP_996816.2:n.10939+18_10939+19dup | |
| NM_206933.3:c.10939+18_10939+19dup | NP_996816.2:n.10939+18_10939+19dup | |
| NM_206933.4:c.10939+18_10939+19dup MANE Select | NP_996816.3:n.10939+18_10939+19dup |