Linked Data
gnomAD v2:
11-20649517-G-GAAT
gnomAD v4:
11-20627971-G-GAAT
MyVariant Identifiers:
chr11:g.20649517_20649518insAAT (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.20627971_20627972insAAT , CM000673.2:g.20627971_20627972insAAT | GRCh38 |
| NC_000011.9:g.20649517_20649518insAAT , CM000673.1:g.20649517_20649518insAAT | GRCh37 |
| NC_000011.8:g.20606093_20606094insAAT | NCBI36 |
| NG_013086.1:g.33572_33573insAAT | |
| NG_013086.2:g.33572_33573insAAT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000525748.6:c.1396-9_1396-8insAAT MANE Select | ENSP00000434364.2:n.1396-9_1396-8insAAT | |
| ENST00000298923.11:c.*693-9_*693-8insAAT | ENSP00000298923.7:n.*693-9_*693-8insAAT | |
| ENST00000525748.5:c.1396-9_1396-8insAAT | ENSP00000434364.1:n.1396-9_1396-8insAAT | |
| NM_004211.3:c.1396-9_1396-8insAAT | NP_004202.2:n.1396-9_1396-8insAAT | |
| XM_005253225.1:c.694-9_694-8insAAT | XP_005253282.1:n.694-9_694-8insAAT | |
| XM_011520473.1:c.1396-9_1396-8insAAT | XP_011518775.1:n.1396-9_1396-8insAAT | |
| NM_001318369.1:c.694-9_694-8insAAT | NP_001305298.1:n.694-9_694-8insAAT | |
| NM_004211.4:c.1396-9_1396-8insAAT | NP_004202.3:n.1396-9_1396-8insAAT | |
| XM_017018544.2:c.520-9_520-8insAAT | XP_016874033.1:n.520-9_520-8insAAT | |
| XM_017018545.2:c.355-9_355-8insAAT | XP_016874034.1:n.355-9_355-8insAAT | |
| NM_001318369.2:c.694-9_694-8insAAT | NP_001305298.1:n.694-9_694-8insAAT | |
| NM_004211.5:c.1396-9_1396-8insAAT MANE Select | NP_004202.4:n.1396-9_1396-8insAAT |