Linked Data
gnomAD v4:
16-2278489-T-TA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2278491dup , CM000678.2:g.2278491dup | GRCh38 |
| NC_000016.9:g.2328492dup , CM000678.1:g.2328492dup | GRCh37 |
| NC_000016.8:g.2268493dup | NCBI36 |
| NG_011790.1:g.67257dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301732.10:c.4548-32dup MANE Select | ENSP00000301732.5:n.4548-32dup | |
| ENST00000301732.9:c.4548-32dup | ENSP00000301732.5:n.4548-32dup | |
| ENST00000382381.7:c.4374-32dup | ENSP00000371818.3:n.4374-32dup | |
| ENST00000566200.1:n.1069-32dup | ||
| NM_001089.2:c.4548-32dup | NP_001080.2:n.4548-32dup | |
| NM_001089.3:c.4548-32dup MANE Select | NP_001080.2:n.4548-32dup |