Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.204190416_204190417insAC , CM000663.2:g.204190416_204190417insAC | GRCh38 |
| NC_000001.10:g.204159544_204159545insAC , CM000663.1:g.204159544_204159545insAC | GRCh37 |
| NC_000001.9:g.202426167_202426168insAC | NCBI36 |
| NG_032151.1:g.11076_11077insTG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367194.5:c.*68_*69insTG MANE Select | ENSP00000356162.4:n.*68_*69insTG | |
| ENST00000367194.4:c.*68_*69insTG | ENSP00000356162.4:n.*68_*69insTG | |
| NM_002256.3:c.*68_*69insTG | NP_002247.3:n.*68_*69insTG | |
| XM_011509525.1:c.*68_*69insTG | XP_011507827.1:n.*68_*69insTG | |
| NM_002256.4:c.*68_*69insTG MANE Select | NP_002247.3:n.*68_*69insTG |