Linked Data
gnomAD v4:
9-12708011-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.12708011C>A , CM000671.2:g.12708011C>A | GRCh38 |
| NC_000009.11:g.12708011C>A , CM000671.1:g.12708011C>A | GRCh37 |
| NC_000009.10:g.12698011C>A | NCBI36 |
| NG_011705.1:g.19626C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000388918.10:c.1276C>A (TYRP1) MANE Select | ENSP00000373570.4:p.Pro426Thr | |
| ENST00000381136.2:c.406C>A (TYRP1) | ENSP00000370528.2:p.Pro136Thr | |
| ENST00000381142.3:n.499-966C>A (TYRP1) | ||
| ENST00000388918.9:c.1276C>A (TYRP1) | ENSP00000373570.4:p.Pro426Thr | |
| ENST00000473504.1:n.341C>A (TYRP1) | ||
| NM_000550.2:c.1276C>A (TYRP1) | NP_000541.1:p.Pro426Thr | |
| NR_125775.1:n.317-7385G>T (LURAP1L-AS1) | ||
| XR_001746372.2:n.1260C>A (TYRP1) | ||
| NM_000550.3:c.1276C>A (TYRP1) MANE Select | NP_000541.1:p.Pro426Thr |