Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.152312247_152312251del , CM000663.2:g.152312247_152312251del | GRCh38 |
| NC_000001.10:g.152284723_152284727del , CM000663.1:g.152284723_152284727del | GRCh37 |
| NC_000001.9:g.150551347_150551351del | NCBI36 |
| NG_016190.1:g.17953_17957del , LRG_1028:g.17953_17957del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368799.2:c.2635_2639del MANE Select | ENSP00000357789.1:p.Arg879Ter | |
| ENST00000368799.1:c.2635_2639del | ENSP00000357789.1:p.Arg879Ter | |
| NM_002016.1:c.2635_2639del , LRG_1028t1:c.2635_2639del | NP_002007.1:p.Arg879Ter | |
| XM_011509329.1:c.2635_2639del | XP_011507631.1:p.Arg879Ter | |
| NM_002016.2:c.2635_2639del MANE Select | NP_002007.1:p.Arg879Ter |