Linked Data
gnomAD v4:
15-38252991-A-AC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.38252997dup , CM000677.2:g.38252997dup | GRCh38 |
| NC_000015.9:g.38545198dup , CM000677.1:g.38545198dup | GRCh37 |
| NC_000015.8:g.36332490dup | NCBI36 |
| NG_008980.1:g.5147dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299084.9:c.-189dup MANE Select | ENSP00000299084.4:n.-189dup | |
| ENST00000299084.8:c.-189dup | ENSP00000299084.4:n.-189dup | |
| ENST00000561205.1:n.150dup | ||
| NM_152594.2:c.-189dup | NP_689807.1:n.-189dup | |
| XM_005254202.2:c.-189dup | XP_005254259.1:n.-189dup | |
| XM_005254203.3:c.-236dup | XP_005254260.1:n.-236dup | |
| XM_005254202.3:c.-189dup | XP_005254259.1:n.-189dup | |
| XR_001751484.1:n.87+575dup | ||
| NM_152594.3:c.-189dup MANE Select | NP_689807.1:n.-189dup |