Linked Data
dbSNP Id:
rs1232009946
MyVariant Identifiers:
chr7:g.128493954_128493955insGGTG (hg19)
chr7:g.128853900_128853901insGGTG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128853900_128853901insGGTG , CM000669.2:g.128853900_128853901insGGTG | GRCh38 |
| NC_000007.13:g.128493954_128493955insGGTG , CM000669.1:g.128493954_128493955insGGTG | GRCh37 |
| NC_000007.12:g.128281190_128281191insGGTG | NCBI36 |
| NG_011807.1:g.28472_28473insGGTG , LRG_870:g.28472_28473insGGTG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000325888.13:c.6484+63_6484+64insGGTG (FLNC) MANE Select | ENSP00000327145.8:n.6484+63_6484+64insGGTG | |
| ENST00000325888.12:c.6484+63_6484+64insGGTG (FLNC) | ENSP00000327145.8:n.6484+63_6484+64insGGTG | |
| ENST00000346177.6:c.6385+63_6385+64insGGTG (FLNC) | ENSP00000344002.6:n.6385+63_6385+64insGGTG | |
| NM_001127487.1:c.6385+63_6385+64insGGTG (FLNC) | NP_001120959.1:n.6385+63_6385+64insGGTG | |
| NM_001458.4:c.6484+63_6484+64insGGTG , LRG_870t1:c.6484+63_6484+64insGGTG (FLNC) | NP_001449.3:n.6484+63_6484+64insGGTG | |
| NR_149055.1:n.103-504_103-503insCACC (FLNC-AS1) | ||
| NM_001127487.2:c.6385+63_6385+64insGGTG (FLNC) | NP_001120959.1:n.6385+63_6385+64insGGTG | |
| NM_001458.5:c.6484+63_6484+64insGGTG (FLNC) MANE Select | NP_001449.3:n.6484+63_6484+64insGGTG |