HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31547540_31547551dup , CM000680.2:g.31547540_31547551dup | GRCh38 |
NC_000018.9:g.29127503_29127514dup , CM000680.1:g.29127503_29127514dup | GRCh37 |
NC_000018.8:g.27381501_27381512dup | NCBI36 |
NG_007072.3:g.54299_54310dup , LRG_397:g.54299_54310dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261590.13:c.*797_*808dup (DSG2) MANE Select | ENSP00000261590.8:n.*797_*808dup | |
ENST00000261590.12:c.*797_*808dup (DSG2) | ENSP00000261590.8:n.*797_*808dup | |
NM_001943.3:c.*797_*808dup , LRG_397t1:c.*797_*808dup (DSG2) | NP_001934.2:n.*797_*808dup | |
NR_045216.1:n.1346-1645_1346-1634dup (DSG2-AS1) | ||
NM_001943.4:c.*797_*808dup (DSG2) | NP_001934.2:n.*797_*808dup | |
NM_001943.5:c.*797_*808dup (DSG2) MANE Select | NP_001934.2:n.*797_*808dup |