Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31547168T= , CM000680.2:g.31547168T= | GRCh38 |
| NC_000018.9:g.29127131T= , CM000680.1:g.29127131T= | GRCh37 |
| NC_000018.8:g.27381129T= | NCBI36 |
| NG_007072.3:g.53927T= , LRG_397:g.53927T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261590.13:c.*425T= (DSG2) MANE Select | ENSP00000261590.8:n.*425T= | |
| ENST00000261590.12:c.*425T= (DSG2) | ENSP00000261590.8:n.*425T= | |
| NM_001943.3:c.*425T= , LRG_397t1:c.*425T= (DSG2) | NP_001934.2:n.*425T= | |
| NR_045216.1:n.1346-1262A= (DSG2-AS1) | ||
| NM_001943.4:c.*425T= (DSG2) | NP_001934.2:n.*425T= | |
| XM_024451095.1:c.*425T= (DSG2) | XP_024306863.1:n.*425T= | |
| NM_001943.5:c.*425T= (DSG2) MANE Select | NP_001934.2:n.*425T= |