Linked Data
dbSNP Id:
rs1678042161
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.193251481dup , CM000663.2:g.193251481dup | GRCh38 |
| NC_000001.10:g.193220611dup , CM000663.1:g.193220611dup | GRCh37 |
| NC_000001.9:g.191487234dup | NCBI36 |
| NG_012691.1:g.134524dup , LRG_507:g.134524dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367435.5:c.*769dup MANE Select | ENSP00000356405.4:n.*769dup | |
| ENST00000635846.1:c.*769dup | ENSP00000490035.1:n.*769dup | |
| ENST00000643006.1:c.*1275dup | ENSP00000496633.1:n.*1275dup | |
| ENST00000367435.3:c.*769dup | ENSP00000356405.3:n.*769dup | |
| NM_024529.4:c.*769dup , LRG_507t1:c.*769dup | NP_078805.3:n.*769dup | |
| NM_024529.5:c.*769dup MANE Select | NP_078805.3:n.*769dup |