Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31548587A>G , CM000680.2:g.31548587A>G | GRCh38 |
| NC_000018.9:g.29128550A>G , CM000680.1:g.29128550A>G | GRCh37 |
| NC_000018.8:g.27382548A>G | NCBI36 |
| NG_007072.3:g.55346A>G , LRG_397:g.55346A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001943.5:c.*1844A>G (DSG2) MANE Select | NP_001934.2:n.*1844A>G |
| ENST00000261590.13:c.*1844A>G (DSG2) MANE Select | ENSP00000261590.8:n.*1844A>G |
| NM_001943.3:c.*1844A>G , LRG_397t1:c.*1844A>G (DSG2) | NP_001934.2:n.*1844A>G |
| NM_001943.4:c.*1844A>G (DSG2) | NP_001934.2:n.*1844A>G |
| NR_045216.1:n.1345+1451T>C (DSG2-AS1) | |
| ENST00000261590.12:c.*1844A>G (DSG2) | ENSP00000261590.8:n.*1844A>G |