HGVS | Genome Assembly |
---|---|
NC_000007.14:g.128852727G>C , CM000669.2:g.128852727G>C | GRCh38 |
NC_000007.13:g.128492781G>C , CM000669.1:g.128492781G>C | GRCh37 |
NC_000007.12:g.128280017G>C | NCBI36 |
NG_011807.1:g.27299G>C , LRG_870:g.27299G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000325888.13:c.5979G>C (FLNC) MANE Select | ENSP00000327145.8:p.Leu1993= | |
ENST00000325888.12:c.5979G>C (FLNC) | ENSP00000327145.8:p.Leu1993= | |
ENST00000346177.6:c.5880G>C (FLNC) | ENSP00000344002.6:p.Leu1960= | |
NM_001127487.1:c.5880G>C (FLNC) | NP_001120959.1:p.Leu1960= | |
NM_001458.4:c.5979G>C , LRG_870t1:c.5979G>C (FLNC) | NP_001449.3:p.Leu1993= | |
NR_149055.1:n.215+558C>G (FLNC-AS1) | ||
NM_001127487.2:c.5880G>C (FLNC) | NP_001120959.1:p.Leu1960= | |
NM_001458.5:c.5979G>C (FLNC) MANE Select | NP_001449.3:p.Leu1993= |