Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.202520106del , CM000664.2:g.202520106del | GRCh38 |
| NC_000002.11:g.203384829del , CM000664.1:g.203384829del | GRCh37 |
| NC_000002.10:g.203093074del | NCBI36 |
| NG_009363.1:g.148780del , LRG_712:g.148780del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000374580.10:c.872del MANE Select | ENSP00000363708.4:p.Leu291Ter | |
| ENST00000638587.1:c.803del | ENSP00000491062.1:p.Leu268Ter | |
| ENST00000374574.2:c.872del | ENSP00000363702.2:p.Leu291Ter | |
| ENST00000374580.8:c.872del | ENSP00000363708.4:p.Leu291Ter | |
| NM_001204.6:c.872del , LRG_712t1:c.872del | NP_001195.2:p.Leu291Ter | |
| XM_011511687.1:c.872del | XP_011509989.1:p.Leu291Ter | |
| XM_011511688.1:c.872del | XP_011509990.1:p.Leu291Ter | |
| NM_001204.7:c.872del MANE Select | NP_001195.2:p.Leu291Ter |