Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23424224_23424225insCT , CM000676.2:g.23424224_23424225insCT | GRCh38 |
| NC_000014.8:g.23893433_23893434insCT , CM000676.1:g.23893433_23893434insCT | GRCh37 |
| NC_000014.7:g.22963273_22963274insCT | NCBI36 |
| NG_007884.1:g.16437_16438insAG , LRG_384:g.16437_16438insAG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355349.4:c.2680-76_2680-75insAG MANE Select | ENSP00000347507.3:n.2680-76_2680-75insAG | |
| ENST00000355349.3:c.2680-76_2680-75insAG | ENSP00000347507.3:n.2680-76_2680-75insAG | |
| NM_000257.3:c.2680-76_2680-75insAG | NP_000248.2:n.2680-76_2680-75insAG | |
| XR_245686.3:n.2786-76_2786-75insAG | ||
| XM_017021340.1:c.2680-76_2680-75insAG | XP_016876829.1:n.2680-76_2680-75insAG | |
| NM_000257.4:c.2680-76_2680-75insAG MANE Select | NP_000248.2:n.2680-76_2680-75insAG |