HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31547192_31547194del , CM000680.2:g.31547192_31547194del | GRCh38 |
NC_000018.9:g.29127155_29127157del , CM000680.1:g.29127155_29127157del | GRCh37 |
NC_000018.8:g.27381153_27381155del | NCBI36 |
NG_007072.3:g.53951_53953del , LRG_397:g.53951_53953del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261590.13:c.*449_*451del (DSG2) MANE Select | ENSP00000261590.8:n.*449_*451del | |
ENST00000261590.12:c.*449_*451del (DSG2) | ENSP00000261590.8:n.*449_*451del | |
NM_001943.3:c.*449_*451del , LRG_397t1:c.*449_*451del (DSG2) | NP_001934.2:n.*449_*451del | |
NR_045216.1:n.1346-1284_1346-1282del (DSG2-AS1) | ||
NM_001943.4:c.*449_*451del (DSG2) | NP_001934.2:n.*449_*451del | |
XM_024451095.1:c.*449_*451del (DSG2) | XP_024306863.1:n.*449_*451del | |
NM_001943.5:c.*449_*451del (DSG2) MANE Select | NP_001934.2:n.*449_*451del |