Linked Data
dbSNP Id:
rs1411973081
gnomAD v4:
1-17336041-GGCTCACACTATGGGT-G
MyVariant Identifiers:
chr1:g.17336042_17336056del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17336044_17336058del , CM000663.2:g.17336044_17336058del | GRCh38 |
| NC_000001.10:g.17662539_17662553del , CM000663.1:g.17662539_17662553del | GRCh37 |
| NC_000001.9:g.17535126_17535140del | NCBI36 |
| NG_023261.2:g.32855_32869del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375448.4:c.341-115_341-101del MANE Select | ENSP00000364597.4:n.341-115_341-101del | |
| NM_012387.2:c.341-115_341-101del | NP_036519.2:n.341-115_341-101del | |
| XM_011541150.1:c.340+2035_340+2049del | XP_011539452.1:n.340+2035_340+2049del | |
| XM_011541151.1:c.341-115_341-101del | XP_011539453.1:n.341-115_341-101del | |
| XM_011541152.1:c.-79-115_-79-101del | XP_011539454.1:n.-79-115_-79-101del | |
| XM_011541153.1:c.341-115_341-101del | XP_011539455.1:n.341-115_341-101del | |
| XM_011541154.1:c.341-115_341-101del | XP_011539456.1:n.341-115_341-101del | |
| XM_011541155.1:c.341-115_341-101del | XP_011539457.1:n.341-115_341-101del | |
| XM_011541156.1:c.341-115_341-101del | XP_011539458.1:n.341-115_341-101del | |
| XM_011541157.1:c.-372-115_-372-101del | XP_011539459.1:n.-372-115_-372-101del | |
| XM_011541154.2:c.341-115_341-101del | XP_011539456.1:n.341-115_341-101del | |
| NM_012387.3:c.341-115_341-101del MANE Select | NP_036519.2:n.341-115_341-101del |