HGVS | Genome Assembly |
---|---|
NC_000006.12:g.159677014_159677015del , CM000668.2:g.159677014_159677015del | GRCh38 |
NC_000006.11:g.160098046_160098047del , CM000668.1:g.160098046_160098047del | GRCh37 |
NC_000006.10:g.160018036_160018037del | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000538183.7:c.*5481_*5482del MANE Select | ENSP00000446252.1:n.*5481_*5482del | |
ENST00000538183.6:c.*5481_*5482del | ENSP00000446252.1:n.*5481_*5482del | |
NM_000636.4:c.*5481_*5482del MANE Select | NP_000627.2:n.*5481_*5482del | |
NM_001322814.2:c.*5481_*5482del | NP_001309743.1:n.*5481_*5482del | |
NM_001322815.2:c.*5481_*5482del | NP_001309744.1:n.*5481_*5482del | |
NM_001322819.2:c.*5481_*5482del | NP_001309748.1:n.*5481_*5482del | |
NM_001322820.2:c.*5481_*5482del | NP_001309749.1:n.*5481_*5482del |