HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31546777_31546780dup , CM000680.2:g.31546777_31546780dup | GRCh38 |
NC_000018.9:g.29126740_29126743dup , CM000680.1:g.29126740_29126743dup | GRCh37 |
NC_000018.8:g.27380738_27380741dup | NCBI36 |
NG_007072.3:g.53536_53539dup , LRG_397:g.53536_53539dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000261590.13:c.*34_*37dup (DSG2) MANE Select | ENSP00000261590.8:n.*34_*37dup | |
ENST00000261590.12:c.*34_*37dup (DSG2) | ENSP00000261590.8:n.*34_*37dup | |
NM_001943.3:c.*34_*37dup , LRG_397t1:c.*34_*37dup (DSG2) | NP_001934.2:n.*34_*37dup | |
NR_045216.1:n.1346-871_1346-868dup (DSG2-AS1) | ||
NM_001943.4:c.*34_*37dup (DSG2) | NP_001934.2:n.*34_*37dup | |
XM_024451095.1:c.*34_*37dup (DSG2) | XP_024306863.1:n.*34_*37dup | |
NM_001943.5:c.*34_*37dup (DSG2) MANE Select | NP_001934.2:n.*34_*37dup |