Linked Data
ClinVar Variation Id:
1373539
ClinVar RCV Id:
RCV001875240
dbSNP Id:
rs1273754617
gnomAD v3:
9-12708011-C-T
gnomAD v4:
9-12708011-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.12708011C>T , CM000671.2:g.12708011C>T | GRCh38 |
| NC_000009.11:g.12708011C>T , CM000671.1:g.12708011C>T | GRCh37 |
| NC_000009.10:g.12698011C>T | NCBI36 |
| NG_011705.1:g.19626C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000388918.10:c.1276C>T (TYRP1) MANE Select | ENSP00000373570.4:p.Pro426Ser | |
| ENST00000381136.2:c.406C>T (TYRP1) | ENSP00000370528.2:p.Pro136Ser | |
| ENST00000381142.3:n.499-966C>T (TYRP1) | ||
| ENST00000388918.9:c.1276C>T (TYRP1) | ENSP00000373570.4:p.Pro426Ser | |
| ENST00000473504.1:n.341C>T (TYRP1) | ||
| NM_000550.2:c.1276C>T (TYRP1) | NP_000541.1:p.Pro426Ser | |
| NR_125775.1:n.317-7385G>A (LURAP1L-AS1) | ||
| XR_001746372.2:n.1260C>T (TYRP1) | ||
| NM_000550.3:c.1276C>T (TYRP1) MANE Select | NP_000541.1:p.Pro426Ser |