HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31547208_31547210dup , CM000680.2:g.31547208_31547210dup | GRCh38 |
NC_000018.9:g.29127171_29127173dup , CM000680.1:g.29127171_29127173dup | GRCh37 |
NC_000018.8:g.27381169_27381171dup | NCBI36 |
NG_007072.3:g.53967_53969dup , LRG_397:g.53967_53969dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261590.13:c.*465_*467dup (DSG2) MANE Select | ENSP00000261590.8:n.*465_*467dup | |
ENST00000261590.12:c.*465_*467dup (DSG2) | ENSP00000261590.8:n.*465_*467dup | |
NM_001943.3:c.*465_*467dup , LRG_397t1:c.*465_*467dup (DSG2) | NP_001934.2:n.*465_*467dup | |
NR_045216.1:n.1346-1304_1346-1302dup (DSG2-AS1) | ||
NM_001943.4:c.*465_*467dup (DSG2) | NP_001934.2:n.*465_*467dup | |
XM_024451095.1:c.*465_*467dup (DSG2) | XP_024306863.1:n.*465_*467dup | |
NM_001943.5:c.*465_*467dup (DSG2) MANE Select | NP_001934.2:n.*465_*467dup |