HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31546820_31546821insT , CM000680.2:g.31546820_31546821insT | GRCh38 |
NC_000018.9:g.29126783_29126784insT , CM000680.1:g.29126783_29126784insT | GRCh37 |
NC_000018.8:g.27380781_27380782insT | NCBI36 |
NG_007072.3:g.53579_53580insT , LRG_397:g.53579_53580insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261590.13:c.*77_*78insT (DSG2) MANE Select | ENSP00000261590.8:n.*77_*78insT | |
ENST00000261590.12:c.*77_*78insT (DSG2) | ENSP00000261590.8:n.*77_*78insT | |
NM_001943.3:c.*77_*78insT , LRG_397t1:c.*77_*78insT (DSG2) | NP_001934.2:n.*77_*78insT | |
NR_045216.1:n.1346-915_1346-914insA (DSG2-AS1) | ||
NM_001943.4:c.*77_*78insT (DSG2) | NP_001934.2:n.*77_*78insT | |
XM_024451095.1:c.*77_*78insT (DSG2) | XP_024306863.1:n.*77_*78insT | |
NM_001943.5:c.*77_*78insT (DSG2) MANE Select | NP_001934.2:n.*77_*78insT |