HGVS | Genome Assembly |
---|---|
NC_000007.14:g.128851474G>T , CM000669.2:g.128851474G>T | GRCh38 |
NC_000007.13:g.128491528G>T , CM000669.1:g.128491528G>T | GRCh37 |
NC_000007.12:g.128278764G>T | NCBI36 |
NG_011807.1:g.26046G>T , LRG_870:g.26046G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000325888.13:c.5688G>T (FLNC) MANE Select | ENSP00000327145.8:p.Val1896= | |
ENST00000325888.12:c.5688G>T (FLNC) | ENSP00000327145.8:p.Val1896= | |
ENST00000346177.6:c.5589G>T (FLNC) | ENSP00000344002.6:p.Val1863= | |
NM_001127487.1:c.5589G>T (FLNC) | NP_001120959.1:p.Val1863= | |
NM_001458.4:c.5688G>T , LRG_870t1:c.5688G>T (FLNC) | NP_001449.3:p.Val1896= | |
NR_149055.1:n.242C>A (FLNC-AS1) | ||
NM_001127487.2:c.5589G>T (FLNC) | NP_001120959.1:p.Val1863= | |
NM_001458.5:c.5688G>T (FLNC) MANE Select | NP_001449.3:p.Val1896= |