HGVS | Genome Assembly |
---|---|
NC_000007.14:g.128858594del , CM000669.2:g.128858594del | GRCh38 |
NC_000007.13:g.128498648del , CM000669.1:g.128498648del | GRCh37 |
NC_000007.12:g.128285884del | NCBI36 |
NG_011807.1:g.33166del , LRG_870:g.33166del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000325888.13:c.*71del (FLNC) MANE Select | ENSP00000327145.8:n.*71del | |
ENST00000325888.12:c.*71del (FLNC) | ENSP00000327145.8:n.*71del | |
ENST00000346177.6:c.*71del (FLNC) | ENSP00000344002.6:n.*71del | |
NM_001127487.1:c.*71del (FLNC) | NP_001120959.1:n.*71del | |
NM_001458.4:c.*71del , LRG_870t1:c.*71del (FLNC) | NP_001449.3:n.*71del | |
NR_149055.1:n.102+3931del (FLNC-AS1) | ||
NM_001127487.2:c.*71del (FLNC) | NP_001120959.1:n.*71del | |
NM_001458.5:c.*71del (FLNC) MANE Select | NP_001449.3:n.*71del |