Revel Score:
ENST00000343849 (MANE Select)
0.889
ENST00000397368
0.889
ClinVar Allele:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.8733962C>T , CM000665.2:g.8733962C>T | GRCh38 |
| NC_000003.11:g.8775648C>T , CM000665.1:g.8775648C>T | GRCh37 |
| NC_000003.10:g.8750648C>T | NCBI36 |
| NG_008797.2:g.5153C>T , LRG_329:g.5153C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343849.3:c.86C>T (CAV3) MANE Select | ENSP00000341940.2:p.Pro29Leu | |
| ENST00000343849.2:c.86C>T (CAV3) | ENSP00000341940.2:p.Pro29Leu | |
| ENST00000397368.2:c.86C>T (CAV3) | ENSP00000380525.2:p.Pro29Leu | |
| ENST00000435138.5:c.64+8497G>A (SSUH2) | ENSP00000412333.1:n.64+8497G>A | |
| ENST00000472766.1:n.127C>T (CAV3) | ||
| ENST00000478513.1:n.335+8497G>A (SSUH2) | ||
| NM_001234.4:c.86C>T (CAV3) | NP_001225.1:p.Pro29Leu | |
| NM_033337.2:c.86C>T , LRG_329t1:c.86C>T (CAV3) | NP_203123.1:p.Pro29Leu | |
| XR_940435.1:n.330+8497G>A (SSUH2) | ||
| XM_017006530.1:c.-283+8497G>A (SSUH2) | XP_016862019.1:n.-283+8497G>A | |
| NM_001234.5:c.86C>T (CAV3) | NP_001225.1:p.Pro29Leu | |
| NM_033337.3:c.86C>T (CAV3) MANE Select | NP_203123.1:p.Pro29Leu |