Linked Data
dbSNP Id:
rs1435087179
gnomAD v2:
X-69247759-TCCAGGACCCCAGGGACCC-T
gnomAD v4:
X-70027909-TCCAGGACCCCAGGGACCC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.70027916_70027933del , CM000685.2:g.70027916_70027933del | GRCh38 |
| NC_000023.10:g.69247766_69247783del , CM000685.1:g.69247766_69247783del | GRCh37 |
| NC_000023.9:g.69164491_69164508del | NCBI36 |
| NG_009809.1:g.416856_416873del | |
| NG_009809.2:g.416850_416867del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374552.9:c.586_603del MANE Select | ENSP00000363680.4:p.Pro196_Gly201del | |
| ENST00000374552.8:c.586_603del | ENSP00000363680.4:p.Pro196_Gly201del | |
| ENST00000374553.6:c.586_603del | ENSP00000363681.2:p.Pro196_Gly201del | |
| ENST00000503592.5:c.190_207del | ENSP00000423037.1:p.Pro64_Gly69del | |
| ENST00000524573.5:c.586_603del | ENSP00000432585.1:p.Pro196_Gly201del | |
| ENST00000616899.1:c.190_207del | ENSP00000481963.1:p.Pro64_Gly69del | |
| NM_001005609.1:c.586_603del | NP_001005609.1:p.Pro196_Gly201del | |
| NM_001005612.2:c.586_603del | NP_001005612.2:p.Pro196_Gly201del | |
| NM_001399.4:c.586_603del | NP_001390.1:p.Pro196_Gly201del | |
| XM_006724630.2:c.586_603del | XP_006724693.1:p.Pro196_Gly201del | |
| XM_011530885.1:c.586_603del | XP_011529187.1:p.Pro196_Gly201del | |
| XM_011530885.2:c.586_603del | XP_011529187.1:p.Pro196_Gly201del | |
| XM_017029336.1:c.586_603del | XP_016884825.1:p.Pro196_Gly201del | |
| NM_001399.5:c.586_603del MANE Select | NP_001390.1:p.Pro196_Gly201del | |
| NM_001005609.2:c.586_603del | NP_001005609.1:p.Pro196_Gly201del | |
| NM_001005612.3:c.586_603del | NP_001005612.2:p.Pro196_Gly201del |