HGVS | Genome Assembly |
---|---|
NC_000005.10:g.148827563_148827567del , CM000667.2:g.148827563_148827567del | GRCh38 |
NC_000005.9:g.148207126_148207130del , CM000667.1:g.148207126_148207130del | GRCh37 |
NC_000005.8:g.148187319_148187323del | NCBI36 |
NG_016421.1:g.5971_5975del | |
NG_016421.2:g.5971_5975del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000305988.6:c.732_736del MANE Select | ENSP00000305372.4:p.Asn244LysfsTer? | |
ENST00000305988.5:c.732_736del | ENSP00000305372.4:p.Asn244LysfsTer? | |
NM_000024.5:c.732_736del | NP_000015.1:p.Asn244LysfsTer? | |
NM_000024.6:c.732_736del MANE Select | NP_000015.2:p.Asn244LysfsTer? |