HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31546774_31546775insG , CM000680.2:g.31546774_31546775insG | GRCh38 |
NC_000018.9:g.29126737_29126738insG , CM000680.1:g.29126737_29126738insG | GRCh37 |
NC_000018.8:g.27380735_27380736insG | NCBI36 |
NG_007072.3:g.53533_53534insG , LRG_397:g.53533_53534insG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261590.13:c.*31_*32insG (DSG2) MANE Select | ENSP00000261590.8:n.*31_*32insG | |
ENST00000261590.12:c.*31_*32insG (DSG2) | ENSP00000261590.8:n.*31_*32insG | |
NM_001943.3:c.*31_*32insG , LRG_397t1:c.*31_*32insG (DSG2) | NP_001934.2:n.*31_*32insG | |
NR_045216.1:n.1346-869_1346-868insC (DSG2-AS1) | ||
NM_001943.4:c.*31_*32insG (DSG2) | NP_001934.2:n.*31_*32insG | |
XM_024451095.1:c.*31_*32insG (DSG2) | XP_024306863.1:n.*31_*32insG | |
NM_001943.5:c.*31_*32insG (DSG2) MANE Select | NP_001934.2:n.*31_*32insG |