Linked Data
gnomAD v4:
4-55125435-C-CTGT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.55125435_55125436insTGT , CM000666.2:g.55125435_55125436insTGT | GRCh38 |
| NC_000004.11:g.55991602_55991603insTGT , CM000666.1:g.55991602_55991603insTGT | GRCh37 |
| NC_000004.10:g.55686359_55686360insTGT | NCBI36 |
| NG_012004.1:g.5160_5161insACA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263923.5:c.-143_-142insACA MANE Select | ENSP00000263923.4:n.-143_-142insACA | |
| ENST00000263923.4:c.-143_-142insACA | ENSP00000263923.4:n.-143_-142insACA | |
| NM_002253.2:c.-143_-142insACA | NP_002244.1:n.-143_-142insACA | |
| NM_002253.3:c.-143_-142insACA | NP_002244.1:n.-143_-142insACA | |
| NM_002253.4:c.-143_-142insACA MANE Select | NP_002244.1:n.-143_-142insACA |