Linked Data
dbSNP Id:
rs2094042688
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.32104888dup , CM000684.2:g.32104888dup | GRCh38 |
| NC_000022.10:g.32500875dup , CM000684.1:g.32500875dup | GRCh37 |
| NC_000022.9:g.30830875dup | NCBI36 |
| NG_017045.1:g.66857dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266088.9:c.1768dup MANE Select | ENSP00000266088.4:p.Ile590AsnfsTer7 | |
| ENST00000266088.8:c.1768dup | ENSP00000266088.4:p.Ile590AsnfsTer7 | |
| ENST00000543737.2:c.1387dup | ENSP00000444898.1:p.Ile463AsnfsTer7 | |
| NM_000343.3:c.1768dup | NP_000334.1:p.Ile590AsnfsTer7 | |
| NM_001256314.1:c.1387dup | NP_001243243.1:p.Ile463AsnfsTer7 | |
| XR_938173.1:n.591+1952dup | ||
| XR_938174.1:n.486+14969dup | ||
| NM_000343.4:c.1768dup MANE Select | NP_000334.1:p.Ile590AsnfsTer7 | |
| NM_001256314.2:c.1387dup | NP_001243243.1:p.Ile463AsnfsTer7 |