HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31546413del , CM000680.2:g.31546413del | GRCh38 |
NC_000018.9:g.29126376del , CM000680.1:g.29126376del | GRCh37 |
NC_000018.8:g.27380374del | NCBI36 |
NG_007072.3:g.53172del , LRG_397:g.53172del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261590.13:c.3027del (DSG2) MANE Select | ENSP00000261590.8:p.Asp1010MetfsTer7 | |
ENST00000261590.12:c.3027del (DSG2) | ENSP00000261590.8:p.Asp1010MetfsTer7 | |
NM_001943.3:c.3027del , LRG_397t1:c.3027del (DSG2) | NP_001934.2:p.Asp1010MetfsTer7 | |
NR_045216.1:n.1346-506del (DSG2-AS1) | ||
NM_001943.4:c.3027del (DSG2) | NP_001934.2:p.Asp1010MetfsTer7 | |
XM_024451095.1:c.2493del (DSG2) | XP_024306863.1:p.Asp832MetfsTer7 | |
NM_001943.5:c.3027del (DSG2) MANE Select | NP_001934.2:p.Asp1010MetfsTer7 |