HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31547222_31547223dup , CM000680.2:g.31547222_31547223dup | GRCh38 |
NC_000018.9:g.29127185_29127186dup , CM000680.1:g.29127185_29127186dup | GRCh37 |
NC_000018.8:g.27381183_27381184dup | NCBI36 |
NG_007072.3:g.53981_53982dup , LRG_397:g.53981_53982dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261590.13:c.*479_*480dup (DSG2) MANE Select | ENSP00000261590.8:n.*479_*480dup | |
ENST00000261590.12:c.*479_*480dup (DSG2) | ENSP00000261590.8:n.*479_*480dup | |
NM_001943.3:c.*479_*480dup , LRG_397t1:c.*479_*480dup (DSG2) | NP_001934.2:n.*479_*480dup | |
NR_045216.1:n.1346-1316_1346-1315dup (DSG2-AS1) | ||
NM_001943.4:c.*479_*480dup (DSG2) | NP_001934.2:n.*479_*480dup | |
XM_024451095.1:c.*479_*480dup (DSG2) | XP_024306863.1:n.*479_*480dup | |
NM_001943.5:c.*479_*480dup (DSG2) MANE Select | NP_001934.2:n.*479_*480dup |