Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.12887160_12887161delinsTG , CM000681.2:g.12887160_12887161delinsTG | GRCh38 |
| NC_000019.9:g.12997974_12997975delinsTG , CM000681.1:g.12997974_12997975delinsTG | GRCh37 |
| NC_000019.8:g.12858974_12858975delinsTG | NCBI36 |
| NG_009292.1:g.1001_1002delinsTG | |
| NG_013087.1:g.5043_5044delinsCA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264834.6:c.-21_-20delinsCA MANE Select | ENSP00000264834.3:n.-21_-20delinsCA | |
| ENST00000264834.4:c.-21_-20delinsCA | ENSP00000264834.3:n.-21_-20delinsCA | |
| NM_006563.3:c.-21_-20delinsCA | NP_006554.1:n.-21_-20delinsCA | |
| NM_006563.4:c.-21_-20delinsCA | NP_006554.1:n.-21_-20delinsCA | |
| NM_006563.5:c.-21_-20delinsCA MANE Select | NP_006554.1:n.-21_-20delinsCA |