Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.116172247dup , CM000685.2:g.116172247dup | GRCh38 |
| NC_000023.10:g.115303500dup , CM000685.1:g.115303500dup | GRCh37 |
| NC_000023.9:g.115217528dup | NCBI36 |
| NG_016326.1:g.6543dup |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000371906.5:c.-34dup MANE Select | ENSP00000360973.4:n.-34dup | |
| ENST00000680409.1:n.435dup | ||
| ENST00000681852.1:c.-34dup | ENSP00000505750.1:n.-34dup | |
| ENST00000371906.4:c.-34dup | ENSP00000360973.4:n.-34dup | |
| NM_000686.4:c.-34dup | NP_000677.2:n.-34dup | |
| XM_011537533.1:c.-34dup | XP_011535835.1:n.-34dup | |
| NM_000686.5:c.-34dup MANE Select | NP_000677.2:n.-34dup | |
| NM_001385624.1:c.-34dup | NP_001372553.1:n.-34dup |