HGVS | Genome Assembly |
---|---|
NC_000007.14:g.128858613del , CM000669.2:g.128858613del | GRCh38 |
NC_000007.13:g.128498667del , CM000669.1:g.128498667del | GRCh37 |
NC_000007.12:g.128285903del | NCBI36 |
NG_011807.1:g.33185del , LRG_870:g.33185del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000325888.13:c.*90del (FLNC) MANE Select | ENSP00000327145.8:n.*90del | |
ENST00000325888.12:c.*90del (FLNC) | ENSP00000327145.8:n.*90del | |
ENST00000346177.6:c.*90del (FLNC) | ENSP00000344002.6:n.*90del | |
NM_001127487.1:c.*90del (FLNC) | NP_001120959.1:n.*90del | |
NM_001458.4:c.*90del , LRG_870t1:c.*90del (FLNC) | NP_001449.3:n.*90del | |
NR_149055.1:n.102+3914del (FLNC-AS1) | ||
NM_001127487.2:c.*90del (FLNC) | NP_001120959.1:n.*90del | |
NM_001458.5:c.*90del (FLNC) MANE Select | NP_001449.3:n.*90del |