Linked Data
MyVariant Identifiers:
chr7:g.128492793C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128852739C>A , CM000669.2:g.128852739C>A | GRCh38 |
| NC_000007.13:g.128492793C>A , CM000669.1:g.128492793C>A | GRCh37 |
| NC_000007.12:g.128280029C>A | NCBI36 |
| NG_011807.1:g.27311C>A , LRG_870:g.27311C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000325888.13:c.5991C>A (FLNC) MANE Select | ENSP00000327145.8:p.Pro1997= | |
| ENST00000325888.12:c.5991C>A (FLNC) | ENSP00000327145.8:p.Pro1997= | |
| ENST00000346177.6:c.5892C>A (FLNC) | ENSP00000344002.6:p.Pro1964= | |
| NM_001127487.1:c.5892C>A (FLNC) | NP_001120959.1:p.Pro1964= | |
| NM_001458.4:c.5991C>A , LRG_870t1:c.5991C>A (FLNC) | NP_001449.3:p.Pro1997= | |
| NR_149055.1:n.215+546G>T (FLNC-AS1) | ||
| NM_001127487.2:c.5892C>A (FLNC) | NP_001120959.1:p.Pro1964= | |
| NM_001458.5:c.5991C>A (FLNC) MANE Select | NP_001449.3:p.Pro1997= |