Revel Score:
ENST00000155840 (MANE Select)
0.789
ENST00000335475
0.789
ClinVar Allele:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2585279A>G , CM000673.2:g.2585279A>G | GRCh38 |
| NC_000011.9:g.2606509A>G , CM000673.1:g.2606509A>G | GRCh37 |
| NC_000011.8:g.2563085A>G | NCBI36 |
| NG_008935.1:g.145289A>G , LRG_287:g.145289A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496887.7:c.771+1734A>G | ENSP00000434560.2:n.771+1734A>G | |
| ENST00000646564.2:c.588+1734A>G | ENSP00000495806.2:n.588+1734A>G | |
| ENST00000155840.12:c.1100A>G MANE Select | ENSP00000155840.2:p.Gln367Arg | |
| ENST00000335475.6:c.719A>G | ENSP00000334497.5:p.Gln240Arg | |
| ENST00000646564.1:c.234+1734A>G | ENSP00000495806.1:n.234+1734A>G | |
| ENST00000155840.9:c.1100A>G | ENSP00000155840.2:p.Gln367Arg | |
| ENST00000335475.5:c.719A>G | ENSP00000334497.5:p.Gln240Arg | |
| NM_000218.2:c.1100A>G , LRG_287t1:c.1100A>G | NP_000209.2:p.Gln367Arg | |
| NM_181798.1:c.719A>G , LRG_287t2:c.719A>G | NP_861463.1:p.Gln240Arg | |
| NM_000218.3:c.1100A>G MANE Select | NP_000209.2:p.Gln367Arg |