Revel Score:
ENST00000496887
0.961
ENST00000155840 (MANE Select)
0.961
ENST00000335475
0.961
gnomAD v2:
gnomAD v3:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2572056C>T , CM000673.2:g.2572056C>T | GRCh38 |
| NC_000011.9:g.2593286C>T , CM000673.1:g.2593286C>T | GRCh37 |
| NC_000011.8:g.2549862C>T | NCBI36 |
| NG_008935.1:g.132066C>T , LRG_287:g.132066C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496887.7:c.466C>T | ENSP00000434560.2:p.Arg156Cys | |
| ENST00000646564.2:c.478-11379C>T | ENSP00000495806.2:n.478-11379C>T | |
| ENST00000155840.12:c.727C>T MANE Select | ENSP00000155840.2:p.Arg243Cys | |
| ENST00000335475.6:c.346C>T | ENSP00000334497.5:p.Arg116Cys | |
| ENST00000646564.1:c.124-11379C>T | ENSP00000495806.1:n.124-11379C>T | |
| ENST00000155840.9:c.727C>T | ENSP00000155840.2:p.Arg243Cys | |
| ENST00000335475.5:c.346C>T | ENSP00000334497.5:p.Arg116Cys | |
| ENST00000496887.6:c.466C>T | ENSP00000434560.1:p.Arg156Cys | |
| NM_000218.2:c.727C>T , LRG_287t1:c.727C>T | NP_000209.2:p.Arg243Cys | |
| NM_181798.1:c.346C>T , LRG_287t2:c.346C>T | NP_861463.1:p.Arg116Cys | |
| NM_000218.3:c.727C>T MANE Select | NP_000209.2:p.Arg243Cys |