ClinVar Variation:
dbSNP:
gnomAD v2:
gnomAD v3:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.87332508A>G , CM000667.2:g.87332508A>G | GRCh38 |
| NC_000005.9:g.86628325A>G , CM000667.1:g.86628325A>G | GRCh37 |
| NC_000005.8:g.86664081A>G | NCBI36 |
| NG_011650.1:g.69175A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274376.11:c.694A>G (RASA1) MANE Select | ENSP00000274376.6:p.Ile232Val | |
| ENST00000645953.1:c.*91-13611T>C (CCNH) | ENSP00000494460.1:n.*91-13611T>C | |
| ENST00000274376.10:c.694A>G (RASA1) | ENSP00000274376.6:p.Ile232Val | |
| ENST00000456692.6:c.163A>G (RASA1) | ENSP00000411221.2:p.Ile55Val | |
| ENST00000506290.1:c.196A>G (RASA1) | ENSP00000420905.1:p.Ile66Val | |
| ENST00000512763.5:c.193A>G (RASA1) | ENSP00000422008.1:p.Ile65Val | |
| ENST00000515800.6:c.694A>G (RASA1) | ENSP00000423395.2:p.Ile232Val | |
| NM_002890.2:c.694A>G (RASA1) | NP_002881.1:p.Ile232Val | |
| NM_022650.2:c.163A>G (RASA1) | NP_072179.1:p.Ile55Val | |
| XM_011543525.1:c.694A>G (RASA1) | XP_011541827.1:p.Ile232Val | |
| XM_011543526.1:c.694A>G (RASA1) | XP_011541828.1:p.Ile232Val | |
| XM_011543527.1:c.694A>G (RASA1) | XP_011541829.1:p.Ile232Val | |
| NM_001364075.1:c.934-19713T>C (CCNH) | NP_001351004.1:n.934-19713T>C | |
| NR_157068.1:n.1448-19713T>C (CCNH) | ||
| NR_157069.1:n.1041-19713T>C (CCNH) | ||
| NR_157070.1:n.1205-19713T>C (CCNH) | ||
| XM_011543525.2:c.694A>G (RASA1) | XP_011541827.1:p.Ile232Val | |
| XM_011543527.3:c.694A>G (RASA1) | XP_011541829.1:p.Ile232Val | |
| NM_001364075.2:c.934-19713T>C (CCNH) | NP_001351004.1:n.934-19713T>C | |
| NM_002890.3:c.694A>G (RASA1) MANE Select | NP_002881.1:p.Ile232Val | |
| NR_157068.2:n.1448-19713T>C (CCNH) | ||
| NR_157069.2:n.1041-19713T>C (CCNH) | ||
| NR_157070.2:n.1205-19713T>C (CCNH) | ||
| NM_022650.3:c.163A>G (RASA1) | NP_072179.1:p.Ile55Val |