Linked Data
dbSNP Id:
rs1190684051
gnomAD v2:
15-48737476-CA-C
gnomAD v3:
15-48445279-CA-C
gnomAD v4:
15-48445279-CA-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48445280del , CM000677.2:g.48445280del | GRCh38 |
| NC_000015.9:g.48737477del , CM000677.1:g.48737477del | GRCh37 |
| NC_000015.8:g.46524769del | NCBI36 |
| NG_008805.2:g.205509del , LRG_778:g.205509del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.5917+96del | ENSP00000453958.2:n.5917+96del | |
| ENST00000674301.2:c.5917+96del | ENSP00000501333.2:n.5917+96del | |
| ENST00000684448.1:n.4591+96del | ||
| ENST00000316623.10:c.5917+96del MANE Select | ENSP00000325527.5:n.5917+96del | |
| ENST00000674301.1:c.916+96del | ENSP00000501333.1:n.916+96del | |
| ENST00000316623.9:c.5917+96del | ENSP00000325527.5:n.5917+96del | |
| ENST00000537463.6:c.*1680+96del | ENSP00000440294.2:n.*1680+96del | |
| ENST00000559133.5:c.1224+96del | ||
| ENST00000560820.1:n.37+96del | ||
| NM_000138.4:c.5917+96del , LRG_778t1:c.5917+96del | NP_000129.3:n.5917+96del | |
| NM_000138.5:c.5917+96del MANE Select | NP_000129.3:n.5917+96del |