Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.119651447_119651448delinsAC , CM000672.2:g.119651447_119651448delinsAC | GRCh38 |
| NC_000010.10:g.121410959_121410960delinsAC , CM000672.1:g.121410959_121410960delinsAC | GRCh37 |
| NC_000010.9:g.121400949_121400950delinsAC | NCBI36 |
| NG_016125.1:g.5078_5079delinsAC , LRG_742:g.5078_5079delinsAC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369085.8:c.-229_-228delinsAC MANE Select | ENSP00000358081.4:n.-229_-228delinsAC | |
| ENST00000369085.7:c.-229_-228delinsAC | ENSP00000358081.3:n.-229_-228delinsAC | |
| NM_004281.3:c.-229_-228delinsAC , LRG_742t1:c.-229_-228delinsAC | NP_004272.2:n.-229_-228delinsAC | |
| XM_005270287.1:c.-229_-228delinsAC | XP_005270344.1:n.-229_-228delinsAC | |
| XM_005270287.2:c.-229_-228delinsAC | XP_005270344.1:n.-229_-228delinsAC | |
| NM_004281.4:c.-229_-228delinsAC MANE Select | NP_004272.2:n.-229_-228delinsAC |