Linked Data
gnomAD v4:
8-64624398-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.64624400del , CM000670.2:g.64624400del | GRCh38 |
| NC_000008.10:g.65536957del , CM000670.1:g.65536957del | GRCh37 |
| NC_000008.9:g.65699511del | NCBI36 |
| NG_008338.1:g.179393del | |
| NG_008338.2:g.179393del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000310193.4:c.259+4del MANE Select | ENSP00000310721.3:n.259+4del | |
| ENST00000310193.3:c.259+4del | ENSP00000310721.3:n.259+4del | |
| NM_004820.3:c.259+4del | NP_004811.1:n.259+4del | |
| NM_001324112.1:c.259+4del | NP_001311041.1:n.259+4del | |
| NM_004820.4:c.259+4del | NP_004811.1:n.259+4del | |
| XM_017014002.1:c.325+4del | XP_016869491.1:n.325+4del | |
| NM_004820.5:c.259+4del MANE Select | NP_004811.1:n.259+4del | |
| NM_001324112.2:c.259+4del | NP_001311041.1:n.259+4del |