HGVS | Genome Assembly |
---|---|
NC_000009.12:g.134843076del , CM000671.2:g.134843076del | GRCh38 |
NC_000009.11:g.137734922del , CM000671.1:g.137734922del | GRCh37 |
NC_000009.10:g.136874743del | NCBI36 |
NG_008030.1:g.206271del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000371820.4:c.*773del | ENSP00000360885.4:n.*773del | |
ENST00000371817.8:c.*773del MANE Select | ENSP00000360882.3:n.*773del | |
ENST00000371817.7:c.*773del | ENSP00000360882.3:n.*773del | |
ENST00000618395.4:c.*773del | ENSP00000481360.1:n.*773del | |
NM_000093.4:c.*773del | NP_000084.3:n.*773del | |
NM_001278074.1:c.*773del | NP_001265003.1:n.*773del | |
NR_103451.2:n.71-22864del | ||
NM_000093.5:c.*773del MANE Select | NP_000084.3:n.*773del |