HGVS | Genome Assembly |
---|---|
NC_000009.12:g.12708150del , CM000671.2:g.12708150del | GRCh38 |
NC_000009.11:g.12708150del , CM000671.1:g.12708150del | GRCh37 |
NC_000009.10:g.12698150del | NCBI36 |
NG_011705.1:g.19765del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000388918.10:c.1408+7del (TYRP1) MANE Select | ENSP00000373570.4:n.1408+7del | |
ENST00000381136.2:c.538+7del (TYRP1) | ENSP00000370528.2:n.538+7del | |
ENST00000381142.3:n.499-827del (TYRP1) | ||
ENST00000388918.9:c.1408+7del (TYRP1) | ENSP00000373570.4:n.1408+7del | |
ENST00000473504.1:n.473+7del (TYRP1) | ||
NM_000550.2:c.1408+7del (TYRP1) | NP_000541.1:n.1408+7del | |
NR_125775.1:n.317-7524del (LURAP1L-AS1) | ||
XR_001746372.2:n.1392+7del (TYRP1) | ||
NM_000550.3:c.1408+7del (TYRP1) MANE Select | NP_000541.1:n.1408+7del |