Linked Data
dbSNP Id:
rs1830587034
gnomAD v3:
9-127825419-TGGCGTCG-T
gnomAD v4:
9-127825419-TGGCGTCG-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.127825422_127825428del , CM000671.2:g.127825422_127825428del | GRCh38 |
| NC_000009.11:g.130587701_130587707del , CM000671.1:g.130587701_130587707del | GRCh37 |
| NC_000009.10:g.129627522_129627528del | NCBI36 |
| NG_009551.1:g.34343_34349del , LRG_589:g.34343_34349del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000480266.6:c.144-69_144-63del | ENSP00000479015.1:n.144-69_144-63del | |
| ENST00000373203.9:c.690-69_690-63del MANE Select | ENSP00000362299.4:n.690-69_690-63del | |
| ENST00000344849.4:c.690-69_690-63del | ENSP00000341917.3:n.690-69_690-63del | |
| ENST00000373203.8:c.690-69_690-63del | ENSP00000362299.4:n.690-69_690-63del | |
| ENST00000480266.5:c.144-69_144-63del | ENSP00000479015.1:n.144-69_144-63del | |
| NM_000118.3:c.690-69_690-63del , LRG_589t1:c.690-69_690-63del | NP_000109.1:n.690-69_690-63del | |
| NM_001114753.2:c.690-69_690-63del , LRG_589t2:c.690-69_690-63del | NP_001108225.1:n.690-69_690-63del | |
| NM_001278138.1:c.144-69_144-63del | NP_001265067.1:n.144-69_144-63del | |
| XR_001746952.2:n.46_52del | ||
| NM_001114753.3:c.690-69_690-63del MANE Select | NP_001108225.1:n.690-69_690-63del | |
| NM_001278138.2:c.144-69_144-63del | NP_001265067.1:n.144-69_144-63del |