Linked Data
gnomAD v4:
5-149977914-AT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149977915del , CM000667.2:g.149977915del | GRCh38 |
| NC_000005.9:g.149357478del , CM000667.1:g.149357478del | GRCh37 |
| NC_000005.8:g.149337671del | NCBI36 |
| NG_007147.2:g.19033del , LRG_684:g.19033del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000690410.1:n.495del | ||
| ENST00000286298.5:c.263del MANE Select | ENSP00000286298.4:p.Met88ArgfsTer3 | |
| ENST00000286298.4:c.263del | ENSP00000286298.4:p.Met88ArgfsTer3 | |
| NM_000112.3:c.263del , LRG_684t1:c.263del | NP_000103.2:p.Met88ArgfsTer3 | |
| XM_017009191.2:c.263del | XP_016864680.1:p.Met88ArgfsTer3 | |
| NM_000112.4:c.263del MANE Select | NP_000103.2:p.Met88ArgfsTer3 |