Linked Data
MyVariant Identifiers:
chr7:g.128497389T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128857335T>G , CM000669.2:g.128857335T>G | GRCh38 |
| NC_000007.13:g.128497389T>G , CM000669.1:g.128497389T>G | GRCh37 |
| NC_000007.12:g.128284625T>G | NCBI36 |
| NG_011807.1:g.31907T>G , LRG_870:g.31907T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000325888.13:c.7779T>G (FLNC) MANE Select | ENSP00000327145.8:p.Thr2593= | |
| ENST00000325888.12:c.7779T>G (FLNC) | ENSP00000327145.8:p.Thr2593= | |
| ENST00000346177.6:c.7680T>G (FLNC) | ENSP00000344002.6:p.Thr2560= | |
| NM_001127487.1:c.7680T>G (FLNC) | NP_001120959.1:p.Thr2560= | |
| NM_001458.4:c.7779T>G , LRG_870t1:c.7779T>G (FLNC) | NP_001449.3:p.Thr2593= | |
| NR_149055.1:n.103-3938A>C (FLNC-AS1) | ||
| NM_001127487.2:c.7680T>G (FLNC) | NP_001120959.1:p.Thr2560= | |
| NM_001458.5:c.7779T>G (FLNC) MANE Select | NP_001449.3:p.Thr2593= |