Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31546705G= , CM000680.2:g.31546705G= | GRCh38 |
| NC_000018.9:g.29126668G= , CM000680.1:g.29126668G= | GRCh37 |
| NC_000018.8:g.27380666G= | NCBI36 |
| NG_007072.3:g.53464G= , LRG_397:g.53464G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261590.13:c.3319G= (DSG2) MANE Select | ENSP00000261590.8:p.Val1107= | |
| ENST00000261590.12:c.3319G= (DSG2) | ENSP00000261590.8:p.Val1107= | |
| NM_001943.3:c.3319G= , LRG_397t1:c.3319G= (DSG2) | NP_001934.2:p.Val1107= | |
| NR_045216.1:n.1346-799C= (DSG2-AS1) | ||
| NM_001943.4:c.3319G= (DSG2) | NP_001934.2:p.Val1107= | |
| XM_024451095.1:c.2785G= (DSG2) | XP_024306863.1:p.Val929= | |
| NM_001943.5:c.3319G= (DSG2) MANE Select | NP_001934.2:p.Val1107= |