Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.152310738_152310739del , CM000663.2:g.152310738_152310739del | GRCh38 |
| NC_000001.10:g.152283214_152283215del , CM000663.1:g.152283214_152283215del | GRCh37 |
| NC_000001.9:g.150549838_150549839del | NCBI36 |
| NG_016190.1:g.19468_19469del , LRG_1028:g.19468_19469del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368799.2:c.4150_4151del MANE Select | ENSP00000357789.1:p.Asp1384GlnfsTer9 | |
| ENST00000368799.1:c.4150_4151del | ENSP00000357789.1:p.Asp1384GlnfsTer9 | |
| NM_002016.1:c.4150_4151del , LRG_1028t1:c.4150_4151del | NP_002007.1:p.Asp1384GlnfsTer9 | |
| XM_011509329.1:c.4150_4151del | XP_011507631.1:p.Asp1384GlnfsTer9 | |
| NM_002016.2:c.4150_4151del MANE Select | NP_002007.1:p.Asp1384GlnfsTer9 |