Linked Data
gnomAD v3:
9-133352881-CAG-C
gnomAD v4:
9-133352881-CAG-C
MyVariant Identifiers:
chr9:g.133352882_133352883del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133352882_133352883del , CM000671.2:g.133352882_133352883del | GRCh38 |
| NC_000009.10:g.135209558_135209559del | NCBI36 |
| NG_008477.1:g.8624_8625del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371974.8:c.516-117_516-116del MANE Select | ENSP00000361042.3:n.516-117_516-116del | |
| ENST00000371974.7:c.516-117_516-116del | ENSP00000361042.3:n.516-117_516-116del | |
| ENST00000437995.1:n.462-153_462-152del | ||
| ENST00000495952.5:n.506-117_506-116del | ||
| ENST00000615505.4:c.189-117_189-116del | ENSP00000482067.1:n.189-117_189-116del | |
| NM_001280787.1:c.189-117_189-116del | NP_001267716.1:n.189-117_189-116del | |
| NM_003172.3:c.516-117_516-116del | NP_003163.1:n.516-117_516-116del | |
| XM_011518942.1:c.189-117_189-116del | XP_011517244.1:n.189-117_189-116del | |
| NM_003172.4:c.516-117_516-116del MANE Select | NP_003163.1:n.516-117_516-116del |