Linked Data
ClinVar Variation Id:
2841775
ClinVar RCV Id:
RCV003721149
dbSNP Id:
rs1349144376
gnomAD v2:
11-17409576-AG-A
gnomAD v4:
11-17388029-AG-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.17388032del , CM000673.2:g.17388032del | GRCh38 |
| NC_000011.9:g.17409579del , CM000673.1:g.17409579del | GRCh37 |
| NC_000011.8:g.17366155del | NCBI36 |
| NG_012446.1:g.5630del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000528992.2:c.-167del | ENSP00000436479.2:n.-167del | |
| ENST00000682350.1:c.-16-184del | ENSP00000508090.1:n.-16-184del | |
| ENST00000682764.1:c.-16-184del | ENSP00000506780.1:n.-16-184del | |
| ENST00000339994.5:c.62del MANE Select | ENSP00000345708.4:p.Pro21LeufsTer? | |
| ENST00000339994.4:c.62del | ENSP00000345708.4:p.Pro21LeufsTer? | |
| ENST00000526912.1:c.-29del | ENSP00000432729.1:n.-29del | |
| ENST00000528731.1:c.-16-184del | ENSP00000434755.1:n.-16-184del | |
| ENST00000528992.1:c.79del | ||
| NM_000525.3:c.62del | NP_000516.3:p.Pro21LeufsTer? | |
| NM_001166290.1:c.-16-184del | NP_001159762.1:n.-16-184del | |
| XM_006718226.2:c.-16-184del | XP_006718289.1:n.-16-184del | |
| XR_930867.1:n.220del | ||
| XM_006718226.3:c.-16-184del | XP_006718289.1:n.-16-184del | |
| XM_017017680.1:c.-16-184del | XP_016873169.1:n.-16-184del | |
| NM_001166290.2:c.-16-184del | NP_001159762.1:n.-16-184del | |
| NM_001377296.1:c.-29del | NP_001364225.1:n.-29del | |
| NM_001377297.1:c.-16-184del | NP_001364226.1:n.-16-184del | |
| NM_000525.4:c.62del MANE Select | NP_000516.3:p.Pro21LeufsTer? |