HGVS | Genome Assembly |
---|---|
NC_000007.14:g.128858628T>A , CM000669.2:g.128858628T>A | GRCh38 |
NC_000007.13:g.128498682T>A , CM000669.1:g.128498682T>A | GRCh37 |
NC_000007.12:g.128285918T>A | NCBI36 |
NG_011807.1:g.33200T>A , LRG_870:g.33200T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000325888.13:c.*105T>A (FLNC) MANE Select | ENSP00000327145.8:n.*105T>A | |
ENST00000325888.12:c.*105T>A (FLNC) | ENSP00000327145.8:n.*105T>A | |
ENST00000346177.6:c.*105T>A (FLNC) | ENSP00000344002.6:n.*105T>A | |
NM_001127487.1:c.*105T>A (FLNC) | NP_001120959.1:n.*105T>A | |
NM_001458.4:c.*105T>A , LRG_870t1:c.*105T>A (FLNC) | NP_001449.3:n.*105T>A | |
NR_149055.1:n.102+3897A>T (FLNC-AS1) | ||
NM_001127487.2:c.*105T>A (FLNC) | NP_001120959.1:n.*105T>A | |
NM_001458.5:c.*105T>A (FLNC) MANE Select | NP_001449.3:n.*105T>A |