Linked Data
dbSNP Id:
rs2046152999
gnomAD v3:
16-16142321-ATTGATT-A
gnomAD v4:
16-16142321-ATTGATT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.16142325_16142330del , CM000678.2:g.16142325_16142330del | GRCh38 |
| NC_000016.9:g.16236182_16236187del , CM000678.1:g.16236182_16236187del | GRCh37 |
| NC_000016.8:g.16143683_16143688del | NCBI36 |
| NG_028268.1:g.197749_197754del | |
| NG_028268.2:g.197749_197754del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000399408.7:c.*1044_*1049del | ENSP00000382340.4:n.*1044_*1049del | |
| ENST00000399410.8:c.*1044_*1049del MANE Select | ENSP00000382342.3:n.*1044_*1049del | |
| ENST00000572882.3:c.*1044_*1049del | ENSP00000461615.2:n.*1044_*1049del | |
| ENST00000676806.1:n.2366_2371del | ||
| ENST00000677164.1:c.*1044_*1049del | ENSP00000502873.1:n.*1044_*1049del | |
| ENST00000678422.1:c.*2737_*2742del | ENSP00000503954.1:n.*2737_*2742del | |
| ENST00000399408.6:c.*1044_*1049del | ENSP00000382340.3:n.*1044_*1049del | |
| ENST00000399410.7:c.*1044_*1049del | ENSP00000382342.3:n.*1044_*1049del | |
| NM_004996.3:c.*1044_*1049del | NP_004987.2:n.*1044_*1049del | |
| XM_011522497.1:c.*1044_*1049del | XP_011520799.1:n.*1044_*1049del | |
| XM_011522498.1:c.*1044_*1049del | XP_011520800.1:n.*1044_*1049del | |
| XM_011522498.2:c.*1044_*1049del | XP_011520800.1:n.*1044_*1049del | |
| XM_017023237.1:c.*1044_*1049del | XP_016878726.1:n.*1044_*1049del | |
| XM_017023238.1:c.*1044_*1049del | XP_016878727.1:n.*1044_*1049del | |
| XM_017023239.1:c.*1044_*1049del | XP_016878728.1:n.*1044_*1049del | |
| XM_017023240.1:c.*1044_*1049del | XP_016878729.1:n.*1044_*1049del | |
| XM_017023241.1:c.*1044_*1049del | XP_016878730.1:n.*1044_*1049del | |
| XM_017023242.1:c.*1044_*1049del | XP_016878731.1:n.*1044_*1049del | |
| NM_004996.4:c.*1044_*1049del MANE Select | NP_004987.2:n.*1044_*1049del |