Linked Data
dbSNP Id:
rs1258628842
gnomAD v2:
7-87171154-TG-T
gnomAD v3:
7-87541838-TG-T
gnomAD v4:
7-87541838-TG-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.87541842del , CM000669.2:g.87541842del | GRCh38 |
| NC_000007.13:g.87171158del , CM000669.1:g.87171158del | GRCh37 |
| NC_000007.12:g.87009094del | NCBI36 |
| NG_011513.1:g.176410del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265724.8:c.2212-375del | ENSP00000265724.3:n.2212-375del | |
| ENST00000622132.5:c.2212-375del MANE Select | ENSP00000478255.1:n.2212-375del | |
| ENST00000265724.7:c.2212-375del | ENSP00000265724.3:n.2212-375del | |
| ENST00000543898.5:c.2020-375del | ENSP00000444095.1:n.2020-375del | |
| ENST00000622132.4:c.2212-375del | ENSP00000478255.1:n.2212-375del | |
| NM_000927.4:c.2212-375del | NP_000918.2:n.2212-375del | |
| NM_001348944.1:c.2212-375del | NP_001335873.1:n.2212-375del | |
| NM_001348945.1:c.2422-375del | NP_001335874.1:n.2422-375del | |
| NM_001348946.1:c.2212-375del | NP_001335875.1:n.2212-375del | |
| NM_001348946.2:c.2212-375del MANE Select | NP_001335875.1:n.2212-375del | |
| NM_000927.5:c.2212-375del | NP_000918.2:n.2212-375del | |
| NM_001348944.2:c.2212-375del | NP_001335873.1:n.2212-375del | |
| NM_001348945.2:c.2422-375del | NP_001335874.1:n.2422-375del |