Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.138945767_138945774del , CM000665.2:g.138945767_138945774del | GRCh38 |
| NC_000003.11:g.138664609_138664616del , CM000665.1:g.138664609_138664616del | GRCh37 |
| NC_000003.10:g.140147299_140147306del | NCBI36 |
| NG_012454.1:g.6367_6374del | |
| NG_029796.1:g.3534_3541del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648323.1:c.949_956del MANE Select | ENSP00000497217.1:p.Pro317GlyfsTer? | |
| ENST00000330315.3:c.949_956del | ENSP00000333188.3:p.Pro317GlyfsTer? | |
| NM_023067.3:c.949_956del | NP_075555.1:p.Pro317GlyfsTer? | |
| NM_023067.4:c.949_956del MANE Select | NP_075555.1:p.Pro317GlyfsTer? |