HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189010688del , CM000664.2:g.189010688del | GRCh38 |
NC_000002.11:g.189875414del , CM000664.1:g.189875414del | GRCh37 |
NC_000002.10:g.189583659del | NCBI36 |
NG_007404.1:g.41316del , LRG_3:g.41316del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000450867.2:c.3953del | ENSP00000415346.2:p.Asp1318ValfsTer? | |
ENST00000304636.9:c.4052del MANE Select | ENSP00000304408.4:p.Asp1351ValfsTer? | |
ENST00000304636.7:c.4052del | ENSP00000304408.3:p.Asp1351ValfsTer? | |
ENST00000317840.9:c.3143del | ENSP00000315243.6:p.Asp1048ValfsTer? | |
ENST00000487010.1:n.1431del | ||
NM_000090.3:c.4052del , LRG_3t1:c.4052del | NP_000081.1:p.Asp1351ValfsTer? | |
NM_000090.4:c.4052del MANE Select | NP_000081.2:p.Asp1351ValfsTer? |