HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31547290_31547292dup , CM000680.2:g.31547290_31547292dup | GRCh38 |
NC_000018.9:g.29127253_29127255dup , CM000680.1:g.29127253_29127255dup | GRCh37 |
NC_000018.8:g.27381251_27381253dup | NCBI36 |
NG_007072.3:g.54049_54051dup , LRG_397:g.54049_54051dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261590.13:c.*547_*549dup (DSG2) MANE Select | ENSP00000261590.8:n.*547_*549dup | |
ENST00000261590.12:c.*547_*549dup (DSG2) | ENSP00000261590.8:n.*547_*549dup | |
NM_001943.3:c.*547_*549dup , LRG_397t1:c.*547_*549dup (DSG2) | NP_001934.2:n.*547_*549dup | |
NR_045216.1:n.1346-1386_1346-1384dup (DSG2-AS1) | ||
NM_001943.4:c.*547_*549dup (DSG2) | NP_001934.2:n.*547_*549dup | |
XM_024451095.1:c.*547_*549dup (DSG2) | XP_024306863.1:n.*547_*549dup | |
NM_001943.5:c.*547_*549dup (DSG2) MANE Select | NP_001934.2:n.*547_*549dup |