Linked Data
gnomAD v4:
7-128858538-TC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128858542del , CM000669.2:g.128858542del | GRCh38 |
| NC_000007.13:g.128498596del , CM000669.1:g.128498596del | GRCh37 |
| NC_000007.12:g.128285832del | NCBI36 |
| NG_011807.1:g.33114del , LRG_870:g.33114del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000325888.13:c.*19del (FLNC) MANE Select | ENSP00000327145.8:n.*19del | |
| ENST00000325888.12:c.*19del (FLNC) | ENSP00000327145.8:n.*19del | |
| ENST00000346177.6:c.*19del (FLNC) | ENSP00000344002.6:n.*19del | |
| NM_001127487.1:c.*19del (FLNC) | NP_001120959.1:n.*19del | |
| NM_001458.4:c.*19del , LRG_870t1:c.*19del (FLNC) | NP_001449.3:n.*19del | |
| NR_149055.1:n.102+3986del (FLNC-AS1) | ||
| NM_001127487.2:c.*19del (FLNC) | NP_001120959.1:n.*19del | |
| NM_001458.5:c.*19del (FLNC) MANE Select | NP_001449.3:n.*19del |