HGVS | Genome Assembly |
---|---|
NC_000009.12:g.12704676_12704677del , CM000671.2:g.12704676_12704677del | GRCh38 |
NC_000009.11:g.12704676_12704677del , CM000671.1:g.12704676_12704677del | GRCh37 |
NC_000009.10:g.12694676_12694677del | NCBI36 |
NG_011705.1:g.16291_16292del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000388918.10:c.1232_1233del (TYRP1) MANE Select | ENSP00000373570.4:p.Phe411Ter | |
ENST00000381136.2:c.362_363del (TYRP1) | ENSP00000370528.2:p.Phe121Ter | |
ENST00000381142.3:n.469_470del (TYRP1) | ||
ENST00000388918.9:c.1232_1233del (TYRP1) | ENSP00000373570.4:p.Phe411Ter | |
NM_000550.2:c.1232_1233del (TYRP1) | NP_000541.1:p.Phe411Ter | |
NR_125775.1:n.317-4050_317-4049del (LURAP1L-AS1) | ||
XR_001746372.2:n.1216_1217del (TYRP1) | ||
NM_000550.3:c.1232_1233del (TYRP1) MANE Select | NP_000541.1:p.Phe411Ter |