Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.48459789del , CM000675.2:g.48459789del | GRCh38 |
| NC_000013.10:g.49033925del , CM000675.1:g.49033925del | GRCh37 |
| NC_000013.9:g.47931926del | NCBI36 |
| NG_009009.1:g.161043del , LRG_517:g.161043del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000267163.6:c.2062del MANE Select | ENSP00000267163.4:p.Leu688CysfsTer8 | |
| ENST00000643064.1:c.194+78346del | ||
| ENST00000650461.1:c.2062del | ENSP00000497193.1:p.Leu688CysfsTer8 | |
| ENST00000267163.4:c.2062del | ENSP00000267163.4:p.Leu688CysfsTer8 | |
| NM_000321.2:c.2062del , LRG_517t1:c.2062del | NP_000312.2:p.Leu688CysfsTer8 | |
| XM_011535171.1:c.1801del | XP_011533473.1:p.Leu601CysfsTer8 | |
| XM_011535171.2:c.1801del | XP_011533473.1:p.Leu601CysfsTer8 | |
| NM_000321.3:c.2062del MANE Select | NP_000312.2:p.Leu688CysfsTer8 |