Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128840123_128840136del , CM000669.2:g.128840123_128840136del | GRCh38 |
| NC_000007.13:g.128480177_128480190del , CM000669.1:g.128480177_128480190del | GRCh37 |
| NC_000007.12:g.128267413_128267426del | NCBI36 |
| NG_011807.1:g.14695_14708del , LRG_870:g.14695_14708del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000325888.13:c.1512_1525del MANE Select | ENSP00000327145.8:p.Gly505GlnfsTer? | |
| ENST00000325888.12:c.1512_1525del | ENSP00000327145.8:p.Gly505GlnfsTer? | |
| ENST00000346177.6:c.1512_1525del | ENSP00000344002.6:p.Gly505GlnfsTer? | |
| NM_001127487.1:c.1512_1525del | NP_001120959.1:p.Gly505GlnfsTer? | |
| NM_001458.4:c.1512_1525del , LRG_870t1:c.1512_1525del | NP_001449.3:p.Gly505GlnfsTer? | |
| NM_001127487.2:c.1512_1525del | NP_001120959.1:p.Gly505GlnfsTer? | |
| NM_001458.5:c.1512_1525del MANE Select | NP_001449.3:p.Gly505GlnfsTer? |