Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.12702424G= , CM000671.2:g.12702424G= | GRCh38 |
| NC_000009.11:g.12702424G= , CM000671.1:g.12702424G= | GRCh37 |
| NC_000009.10:g.12692424G= | NCBI36 |
| NG_011705.1:g.14039G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000550.3:c.1067G= (TYRP1) MANE Select | NP_000541.1:p.Arg356= |
| ENST00000388918.10:c.1067G= (TYRP1) MANE Select | ENSP00000373570.4:p.Arg356= |
| NM_000550.2:c.1067G= (TYRP1) | NP_000541.1:p.Arg356= |
| NR_125775.1:n.317-1798C= (LURAP1L-AS1) | |
| ENST00000381136.2:c.197G= (TYRP1) | ENSP00000370528.2:p.Arg66= |
| ENST00000381142.3:n.304G= (TYRP1) | |
| ENST00000388918.9:c.1067G= (TYRP1) | ENSP00000373570.4:p.Arg356= |
| ENST00000470909.1:n.325G= (TYRP1) | |
| XR_001746372.2:n.1051G= (TYRP1) |