Linked Data
dbSNP Id:
rs745506317
ExAC:
7:128363213 GC / G
gnomAD v2:
7-128363213-GC-G
gnomAD v3:
7-128723159-GC-G
gnomAD v4:
7-128723159-GC-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128723161del , CM000669.2:g.128723161del | GRCh38 |
| NC_000007.13:g.128363215del , CM000669.1:g.128363215del | GRCh37 |
| NC_000007.12:g.128150451del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000621392.5:c.688-36del MANE Select | ENSP00000477573.2:n.688-36del | |
| ENST00000315184.9:c.688-36del | ENSP00000326652.4:n.688-36del | |
| ENST00000466842.1:c.256-36del | ENSP00000417930.1:n.256-36del | |
| ENST00000469348.5:n.547-36del | ||
| ENST00000471558.5:c.688-36del | ENSP00000418672.1:n.688-36del | |
| ENST00000484425.6:c.259-36del | ENSP00000418591.2:n.259-36del | |
| ENST00000485070.5:c.391-36del | ENSP00000418192.1:n.391-36del | |
| ENST00000493738.5:n.644-36del | ||
| ENST00000621392.4:c.391-36del | ENSP00000477573.1:n.391-36del | |
| NM_001282788.1:c.688-36del | NP_001269717.1:n.688-36del | |
| NM_001282789.1:c.391-36del | NP_001269718.1:n.391-36del | |
| NM_032599.3:c.688-36del | NP_115988.1:n.688-36del | |
| NR_104242.1:n.788-36del | ||
| NR_104243.1:n.677-36del | ||
| XM_017012743.2:c.688-36del | XP_016868232.1:n.688-36del | |
| XR_002956499.1:n.739-36del | ||
| NM_001282788.2:c.688-36del | NP_001269717.1:n.688-36del | |
| NM_001282789.2:c.391-36del | NP_001269718.1:n.391-36del | |
| NM_032599.4:c.688-36del | NP_115988.1:n.688-36del | |
| NR_104242.2:n.739-36del | ||
| NR_104243.2:n.677-36del | ||
| NM_001282788.3:c.688-36del MANE Select | NP_001269717.1:n.688-36del |