Linked Data
gnomAD v4:
4-24800254-C-CT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.24800254_24800255insT , CM000666.2:g.24800254_24800255insT | GRCh38 |
| NC_000004.11:g.24801876_24801877insT , CM000666.1:g.24801876_24801877insT | GRCh37 |
| NC_000004.10:g.24410974_24410975insT | NCBI36 |
| NG_012213.1:g.9792_9793insT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382120.4:c.*10_*11insT MANE Select | ENSP00000371554.3:n.*10_*11insT | |
| ENST00000382120.3:c.*10_*11insT | ENSP00000371554.3:n.*10_*11insT | |
| NM_003102.2:c.*10_*11insT | NP_003093.2:n.*10_*11insT | |
| XR_427488.1:n.923_924insT | ||
| NM_003102.3:c.*10_*11insT | NP_003093.2:n.*10_*11insT | |
| NM_003102.4:c.*10_*11insT MANE Select | NP_003093.2:n.*10_*11insT |