Linked Data
gnomAD v4:
15-38252926-T-TC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.38252929dup , CM000677.2:g.38252929dup | GRCh38 |
| NC_000015.9:g.38545130dup , CM000677.1:g.38545130dup | GRCh37 |
| NC_000015.8:g.36332422dup | NCBI36 |
| NG_008980.1:g.5079dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299084.9:c.-257dup MANE Select | ENSP00000299084.4:n.-257dup | |
| ENST00000299084.8:c.-257dup | ENSP00000299084.4:n.-257dup | |
| ENST00000561205.1:n.82dup | ||
| NM_152594.2:c.-257dup | NP_689807.1:n.-257dup | |
| XM_005254202.2:c.-257dup | XP_005254259.1:n.-257dup | |
| XM_005254203.3:c.-304dup | XP_005254260.1:n.-304dup | |
| XM_005254202.3:c.-257dup | XP_005254259.1:n.-257dup | |
| XR_001751484.1:n.87+640dup | ||
| NM_152594.3:c.-257dup MANE Select | NP_689807.1:n.-257dup |