Linked Data
ClinVar Variation Id:
936729
ClinVar RCV Id:
RCV001205586
dbSNP Id:
rs1257362365
gnomAD v4:
18-23545062-AC-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.23545063del , CM000680.2:g.23545063del | GRCh38 |
| NC_000018.9:g.21125027del , CM000680.1:g.21125027del | GRCh37 |
| NC_000018.8:g.19379025del | NCBI36 |
| NG_012795.1:g.46555del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000269228.10:c.1844del MANE Select | ENSP00000269228.4:p.Arg615LeufsTer11 | |
| ENST00000269228.9:c.1844del | ENSP00000269228.4:p.Arg615LeufsTer11 | |
| ENST00000540608.5:n.1758del | ||
| ENST00000591051.1:c.922del | ||
| NM_000271.4:c.1844del | NP_000262.2:p.Arg615LeufsTer11 | |
| XM_005258277.1:c.1895del | XP_005258334.1:p.Arg632LeufsTer11 | |
| XM_005258278.3:c.1895del | XP_005258335.1:p.Arg632LeufsTer11 | |
| XM_005258279.1:c.1844del | XP_005258336.1:p.Arg615LeufsTer11 | |
| XM_006722479.2:c.1895del | XP_006722542.1:p.Arg632LeufsTer11 | |
| XM_011526015.1:c.1430del | XP_011524317.1:p.Arg477LeufsTer11 | |
| XM_005258278.5:c.1895del | XP_005258335.1:p.Arg632LeufsTer11 | |
| XM_005258279.2:c.1844del | XP_005258336.1:p.Arg615LeufsTer11 | |
| XM_006722479.3:c.1895del | XP_006722542.1:p.Arg632LeufsTer11 | |
| XM_017025784.1:c.1895del | XP_016881273.1:p.Arg632LeufsTer11 | |
| XM_017025785.1:c.1895del | XP_016881274.1:p.Arg632LeufsTer11 | |
| XM_017025786.1:c.1844del | XP_016881275.1:p.Arg615LeufsTer11 | |
| XM_017025787.1:c.1844del | XP_016881276.1:p.Arg615LeufsTer11 | |
| NM_000271.5:c.1844del MANE Select | NP_000262.2:p.Arg615LeufsTer11 |