Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.76346173dup , CM000674.2:g.76346173dup | GRCh38 |
| NC_000012.11:g.76739953dup , CM000674.1:g.76739953dup | GRCh37 |
| NC_000012.10:g.75264084dup | NCBI36 |
| NG_016357.1:g.7270dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650064.2:c.1812dup MANE Select | ENSP00000497413.1:p.Asn605Ter | |
| ENST00000393262.3:c.1812dup | ENSP00000376946.3:p.Asn605Ter | |
| NM_024685.3:c.1812dup | NP_078961.3:p.Asn605Ter | |
| NM_024685.4:c.1812dup MANE Select | NP_078961.3:p.Asn605Ter |