Linked Data
ClinVar Variation Id:
211951
ClinVar RCV Id:
RCV003765233
dbSNP Id:
rs755660222
ExAC:
14:77767570 AC / A
gnomAD v2:
14-77767570-AC-A
gnomAD v4:
14-77301227-AC-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.77301229del , CM000676.2:g.77301229del | GRCh38 |
| NC_000014.8:g.77767572del , CM000676.1:g.77767572del | GRCh37 |
| NC_000014.7:g.76837325del | NCBI36 |
| NG_008897.1:g.24655del , LRG_844:g.24655del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000553863.6:c.131del | ENSP00000508202.1:p.Gly44ValfsTer9 | |
| ENST00000556394.2:c.358-1667del | ENSP00000451967.2:n.358-1667del | |
| ENST00000556880.6:n.702del | ||
| ENST00000557289.2:c.22del | ||
| ENST00000682247.1:c.678del | ENSP00000507213.1:p.Trp226CysfsTer6 | |
| ENST00000682382.1:c.496-2457del | ||
| ENST00000682395.1:n.407del | ||
| ENST00000682459.1:n.342del | ||
| ENST00000682467.1:c.678del | ENSP00000508062.1:p.Trp226CysfsTer6 | |
| ENST00000682795.1:c.678del | ENSP00000507574.1:p.Trp226CysfsTer6 | |
| ENST00000682895.1:n.394del | ||
| ENST00000682955.1:n.212-2457del | ||
| ENST00000683167.1:c.22del | ||
| ENST00000683188.1:c.343-1667del | ||
| ENST00000683300.1:c.109+3464del | ENSP00000507630.1:n.109+3464del | |
| ENST00000683328.1:c.109+3464del | ENSP00000508096.1:n.109+3464del | |
| ENST00000683380.1:n.342del | ||
| ENST00000683398.1:c.22del | ||
| ENST00000683551.1:c.109+1607del | ||
| ENST00000683828.1:c.525+1607del | ||
| ENST00000684259.1:n.529del | ||
| ENST00000684549.1:n.368-1667del | ||
| ENST00000684554.1:c.22del | ||
| ENST00000261534.9:c.678del MANE Select | ENSP00000261534.4:p.Trp226CysfsTer6 | |
| ENST00000261534.8:c.678del | ENSP00000261534.4:p.Trp226CysfsTer6 | |
| ENST00000452340.7:n.701del | ||
| ENST00000553863.5:n.342del | ||
| ENST00000554948.1:c.405del | ENSP00000452060.1:p.Trp135CysfsTer? | |
| ENST00000555675.5:n.394del | ||
| ENST00000556326.5:c.*344del | ENSP00000450630.1:n.*344del | |
| ENST00000557289.1:c.56-1667del | ENSP00000451115.1:n.56-1667del | |
| NM_013382.5:c.678del , LRG_844t1:c.678del | NP_037514.2:p.Trp226CysfsTer6 | |
| XM_011536675.1:c.678del | XP_011534977.1:p.Trp226CysfsTer6 | |
| XM_011536676.1:c.345del | XP_011534978.1:p.Trp115CysfsTer6 | |
| XM_011536677.1:c.547+3464del | XP_011534979.1:n.547+3464del | |
| XM_011536678.1:c.678del | XP_011534980.1:p.Trp226CysfsTer6 | |
| XM_011536679.1:c.-90-1667del | XP_011534981.1:n.-90-1667del | |
| XM_011536680.1:c.678del | XP_011534982.1:p.Trp226CysfsTer6 | |
| XR_943416.1:n.881del | ||
| XM_011536675.2:c.678del | XP_011534977.1:p.Trp226CysfsTer6 | |
| XM_011536676.2:c.345del | XP_011534978.1:p.Trp115CysfsTer6 | |
| XM_011536677.3:c.547+3464del | XP_011534979.1:n.547+3464del | |
| XR_001750279.1:n.878del | ||
| XR_001750282.1:n.882del | ||
| XR_943416.3:n.879del | ||
| NM_013382.6:c.678del | NP_037514.2:p.Trp226CysfsTer6 | |
| NM_013382.7:c.678del MANE Select | NP_037514.2:p.Trp226CysfsTer6 |