Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.118111384_118111386dup , CM000670.2:g.118111384_118111386dup | GRCh38 |
| NC_000008.10:g.119123623_119123625dup , CM000670.1:g.119123623_119123625dup | GRCh37 |
| NC_000008.9:g.119192804_119192806dup | NCBI36 |
| NG_007455.2:g.5440_5442dup , LRG_493:g.5440_5442dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378204.7:c.-334_-332dup MANE Select | ENSP00000367446.3:n.-334_-332dup | |
| ENST00000378204.6:c.-334_-332dup | ENSP00000367446.2:n.-334_-332dup | |
| NM_000127.2:c.-334_-332dup , LRG_493t1:c.-334_-332dup | NP_000118.2:n.-334_-332dup | |
| NM_000127.3:c.-334_-332dup MANE Select | NP_000118.2:n.-334_-332dup |