Linked Data
gnomAD v4:
5-157241469-TG-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.157241470del , CM000667.2:g.157241470del | GRCh38 |
| NC_000005.9:g.156668480del , CM000667.1:g.156668480del | GRCh37 |
| NC_000005.8:g.156601058del | NCBI36 |
| NG_016276.1:g.65574del , LRG_189:g.65574del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696962.1:c.852-176del | ENSP00000513001.1:n.852-176del | |
| ENST00000422843.8:c.986-176del MANE Select | ENSP00000398655.4:n.986-176del | |
| ENST00000422843.7:c.986-176del | ENSP00000398655.3:n.986-176del | |
| ENST00000519402.5:n.2395del | ||
| ENST00000520173.1:n.104-176del | ||
| NM_005546.3:c.986-176del , LRG_189t1:c.986-176del | NP_005537.3:n.986-176del | |
| XM_017009443.1:c.611-176del | XP_016864932.1:n.611-176del | |
| NM_005546.4:c.986-176del MANE Select | NP_005537.3:n.986-176del |