Linked Data
dbSNP Id:
rs1554754077
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.136673711dup , CM000671.2:g.136673711dup | GRCh38 |
| NC_000009.11:g.139568163dup , CM000671.1:g.139568163dup | GRCh37 |
| NC_000009.10:g.138687984dup | NCBI36 |
| NG_008090.1:g.18750dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371696.7:c.*42dup MANE Select | ENSP00000360761.2:n.*42dup | |
| ENST00000371694.7:c.*42dup | ENSP00000360759.3:n.*42dup | |
| ENST00000371696.6:c.*42dup | ENSP00000360761.2:n.*42dup | |
| ENST00000472820.1:n.807dup | ||
| ENST00000538402.1:c.*42dup | ENSP00000438919.1:n.*42dup | |
| NM_001012727.1:c.*42dup | NP_001012745.1:n.*42dup | |
| NM_006412.3:c.*42dup | NP_006403.2:n.*42dup | |
| NM_006412.4:c.*42dup MANE Select | NP_006403.2:n.*42dup | |
| NM_001012727.2:c.*42dup | NP_001012745.1:n.*42dup |