Revel Score:
ENST00000155840 (MANE Select)
0.969
ENST00000335475
0.969
ClinVar Allele:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2585276G>C , CM000673.2:g.2585276G>C | GRCh38 |
| NC_000011.9:g.2606506G>C , CM000673.1:g.2606506G>C | GRCh37 |
| NC_000011.8:g.2563082G>C | NCBI36 |
| NG_008935.1:g.145286G>C , LRG_287:g.145286G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496887.7:c.771+1731G>C | ENSP00000434560.2:n.771+1731G>C | |
| ENST00000646564.2:c.588+1731G>C | ENSP00000495806.2:n.588+1731G>C | |
| ENST00000155840.12:c.1097G>C MANE Select | ENSP00000155840.2:p.Arg366Pro | |
| ENST00000335475.6:c.716G>C | ENSP00000334497.5:p.Arg239Pro | |
| ENST00000646564.1:c.234+1731G>C | ENSP00000495806.1:n.234+1731G>C | |
| ENST00000155840.9:c.1097G>C | ENSP00000155840.2:p.Arg366Pro | |
| ENST00000335475.5:c.716G>C | ENSP00000334497.5:p.Arg239Pro | |
| NM_000218.2:c.1097G>C , LRG_287t1:c.1097G>C | NP_000209.2:p.Arg366Pro | |
| NM_181798.1:c.716G>C , LRG_287t2:c.716G>C | NP_861463.1:p.Arg239Pro | |
| NM_000218.3:c.1097G>C MANE Select | NP_000209.2:p.Arg366Pro |