Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.8745529dup , CM000665.2:g.8745529dup | GRCh38 |
| NC_000003.11:g.8787215dup , CM000665.1:g.8787215dup | GRCh37 |
| NC_000003.10:g.8762215dup | NCBI36 |
| NG_008797.2:g.16720dup , LRG_329:g.16720dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343849.3:c.118dup MANE Select | ENSP00000341940.2:p.Asp40GlyfsTer3 | |
| ENST00000343849.2:c.118dup | ENSP00000341940.2:p.Asp40GlyfsTer3 | |
| ENST00000397368.2:c.118dup | ENSP00000380525.2:p.Asp40GlyfsTer3 | |
| ENST00000472766.1:n.155+11539dup | ||
| NM_001234.4:c.118dup | NP_001225.1:p.Asp40GlyfsTer3 | |
| NM_033337.2:c.118dup , LRG_329t1:c.118dup | NP_203123.1:p.Asp40GlyfsTer3 | |
| NM_001234.5:c.118dup | NP_001225.1:p.Asp40GlyfsTer3 | |
| NM_033337.3:c.118dup MANE Select | NP_203123.1:p.Asp40GlyfsTer3 |