HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31546882_31546884dup , CM000680.2:g.31546882_31546884dup | GRCh38 |
NC_000018.9:g.29126845_29126847dup , CM000680.1:g.29126845_29126847dup | GRCh37 |
NC_000018.8:g.27380843_27380845dup | NCBI36 |
NG_007072.3:g.53641_53643dup , LRG_397:g.53641_53643dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261590.13:c.*139_*141dup (DSG2) MANE Select | ENSP00000261590.8:n.*139_*141dup | |
ENST00000261590.12:c.*139_*141dup (DSG2) | ENSP00000261590.8:n.*139_*141dup | |
NM_001943.3:c.*139_*141dup , LRG_397t1:c.*139_*141dup (DSG2) | NP_001934.2:n.*139_*141dup | |
NR_045216.1:n.1346-977_1346-975dup (DSG2-AS1) | ||
NM_001943.4:c.*139_*141dup (DSG2) | NP_001934.2:n.*139_*141dup | |
XM_024451095.1:c.*139_*141dup (DSG2) | XP_024306863.1:n.*139_*141dup | |
NM_001943.5:c.*139_*141dup (DSG2) MANE Select | NP_001934.2:n.*139_*141dup |