Linked Data
dbSNP Id:
rs1435767751
gnomAD v2:
11-116626275-CA-C
gnomAD v3:
11-116755559-CA-C
gnomAD v4:
11-116755559-CA-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.116755560del , CM000673.2:g.116755560del | GRCh38 |
| NC_000011.9:g.116626276del , CM000673.1:g.116626276del | GRCh37 |
| NC_000011.8:g.116131486del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260210.5:c.1766+1586del MANE Select | ENSP00000260210.3:n.1766+1586del | |
| ENST00000260210.4:c.1766+1586del | ENSP00000260210.3:n.1766+1586del | |
| ENST00000375445.7:c.1364+1586del | ENSP00000364594.3:n.1364+1586del | |
| ENST00000419189.1:c.541+1586del | ||
| NM_001159736.1:c.1364+1586del | NP_001153208.1:n.1364+1586del | |
| NM_032725.3:c.1766+1586del | NP_116114.1:n.1766+1586del | |
| XM_011543035.1:c.1667+1586del | XP_011541337.1:n.1667+1586del | |
| XM_011543035.2:c.1667+1586del | XP_011541337.1:n.1667+1586del | |
| NM_032725.4:c.1766+1586del MANE Select | NP_116114.1:n.1766+1586del | |
| NM_001159736.2:c.1364+1586del | NP_001153208.1:n.1364+1586del |