HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31547310_31547312del , CM000680.2:g.31547310_31547312del | GRCh38 |
NC_000018.9:g.29127273_29127275del , CM000680.1:g.29127273_29127275del | GRCh37 |
NC_000018.8:g.27381271_27381273del | NCBI36 |
NG_007072.3:g.54069_54071del , LRG_397:g.54069_54071del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261590.13:c.*567_*569del (DSG2) MANE Select | ENSP00000261590.8:n.*567_*569del | |
ENST00000261590.12:c.*567_*569del (DSG2) | ENSP00000261590.8:n.*567_*569del | |
NM_001943.3:c.*567_*569del , LRG_397t1:c.*567_*569del (DSG2) | NP_001934.2:n.*567_*569del | |
NR_045216.1:n.1346-1404_1346-1402del (DSG2-AS1) | ||
NM_001943.4:c.*567_*569del (DSG2) | NP_001934.2:n.*567_*569del | |
XM_024451095.1:c.*567_*569del (DSG2) | XP_024306863.1:n.*567_*569del | |
NM_001943.5:c.*567_*569del (DSG2) MANE Select | NP_001934.2:n.*567_*569del |