HGVS | Genome Assembly |
---|---|
NC_000023.11:g.68829877_68829890del , CM000685.2:g.68829877_68829890del | GRCh38 |
NC_000023.10:g.68049720_68049733del , CM000685.1:g.68049720_68049733del | GRCh37 |
NC_000023.9:g.67966445_67966458del | NCBI36 |
NG_008887.1:g.5881_5894del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000204961.5:c.101_114del MANE Select | ENSP00000204961.4:p.Pro34LeufsTer? | |
ENST00000204961.4:c.101_114del | ENSP00000204961.4:p.Pro34LeufsTer? | |
NM_004429.4:c.101_114del | NP_004420.1:p.Pro34LeufsTer? | |
NM_004429.5:c.101_114del MANE Select | NP_004420.1:p.Pro34LeufsTer? |