Linked Data
ClinVar Variation Id:
1608498
ClinVar RCV Id:
RCV002147481
dbSNP Id:
rs2112421478
gnomAD v4:
5-87349227-C-T
MyVariant Identifiers:
chr5:g.86645044C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.87349227C>T , CM000667.2:g.87349227C>T | GRCh38 |
| NC_000005.9:g.86645044C>T , CM000667.1:g.86645044C>T | GRCh37 |
| NC_000005.8:g.86680800C>T | NCBI36 |
| NG_011650.1:g.85894C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274376.11:c.1116C>T (RASA1) MANE Select | ENSP00000274376.6:p.Cys372= | |
| ENST00000645953.1:c.*91-30330G>A (CCNH) | ENSP00000494460.1:n.*91-30330G>A | |
| ENST00000274376.10:c.1116C>T (RASA1) | ENSP00000274376.6:p.Cys372= | |
| ENST00000456692.6:c.585C>T (RASA1) | ENSP00000411221.2:p.Cys195= | |
| ENST00000506290.1:c.618C>T (RASA1) | ENSP00000420905.1:p.Cys206= | |
| ENST00000509953.1:n.219C>T (RASA1) | ||
| ENST00000512763.5:c.615C>T (RASA1) | ENSP00000422008.1:p.Cys205= | |
| ENST00000515800.6:c.1116C>T (RASA1) | ENSP00000423395.2:p.Cys372= | |
| NM_002890.2:c.1116C>T (RASA1) | NP_002881.1:p.Cys372= | |
| NM_022650.2:c.585C>T (RASA1) | NP_072179.1:p.Cys195= | |
| XM_011543525.1:c.1116C>T (RASA1) | XP_011541827.1:p.Cys372= | |
| XM_011543526.1:c.1116C>T (RASA1) | XP_011541828.1:p.Cys372= | |
| XM_011543527.1:c.1116C>T (RASA1) | XP_011541829.1:p.Cys372= | |
| NM_001364075.1:c.934-36432G>A (CCNH) | NP_001351004.1:n.934-36432G>A | |
| NR_157068.1:n.1448-36432G>A (CCNH) | ||
| NR_157069.1:n.1041-36432G>A (CCNH) | ||
| NR_157070.1:n.1205-36432G>A (CCNH) | ||
| XM_011543525.2:c.1116C>T (RASA1) | XP_011541827.1:p.Cys372= | |
| XM_011543527.3:c.1116C>T (RASA1) | XP_011541829.1:p.Cys372= | |
| NM_001364075.2:c.934-36432G>A (CCNH) | NP_001351004.1:n.934-36432G>A | |
| NM_002890.3:c.1116C>T (RASA1) MANE Select | NP_002881.1:p.Cys372= | |
| NR_157068.2:n.1448-36432G>A (CCNH) | ||
| NR_157069.2:n.1041-36432G>A (CCNH) | ||
| NR_157070.2:n.1205-36432G>A (CCNH) | ||
| NM_022650.3:c.585C>T (RASA1) | NP_072179.1:p.Cys195= |