HGVS | Genome Assembly |
---|---|
NC_000005.10:g.140114273_140114346del , CM000667.2:g.140114273_140114346del | GRCh38 |
NC_000005.9:g.139493858_139493931del , CM000667.1:g.139493858_139493931del | GRCh37 |
NC_000005.8:g.139474042_139474115del | NCBI36 |
NG_041813.1:g.5151_5224del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331327.5:c.92_165del MANE Select | ENSP00000332706.3:p.Gly31AlafsTer? | |
ENST00000505703.2:c.92_165del | ENSP00000498560.1:p.Gly31AlafsTer? | |
ENST00000651386.1:c.92_165del | ENSP00000499133.1:p.Gly31AlafsTer? | |
ENST00000331327.4:c.92_165del | ENSP00000332706.3:p.Gly31AlafsTer? | |
NM_005859.4:c.92_165del | NP_005850.1:p.Gly31AlafsTer? | |
NM_005859.5:c.92_165del MANE Select | NP_005850.1:p.Gly31AlafsTer? |