Linked Data
gnomAD v4:
5-1411181-G-GC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1411186dup , CM000667.2:g.1411186dup | GRCh38 |
| NC_000005.9:g.1411301dup , CM000667.1:g.1411301dup | GRCh37 |
| NC_000005.8:g.1464301dup | NCBI36 |
| NG_015885.1:g.39247dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270349.12:c.1269+61dup MANE Select | ENSP00000270349.9:n.1269+61dup | |
| ENST00000270349.11:c.1269+61dup | ENSP00000270349.9:n.1269+61dup | |
| NM_001044.4:c.1269+61dup | NP_001035.1:n.1269+61dup | |
| NM_001044.5:c.1269+61dup MANE Select | NP_001035.1:n.1269+61dup |