Revel Score:
ENST00000380746
0.907
ENST00000321117 (MANE Select)
0.907
ENST00000264709
0.907
ENST00000402667
0.907
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.25234374G>C , CM000664.2:g.25234374G>C | GRCh38 |
| NC_000002.11:g.25457243G>C , CM000664.1:g.25457243G>C | GRCh37 |
| NC_000002.10:g.25310747G>C | NCBI36 |
| NG_029465.2:g.113217C>G , LRG_459:g.113217C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000474887.6:c.893C>G | ||
| ENST00000683393.1:c.1790C>G | ENSP00000508654.1:n.1790C>G | |
| ENST00000683760.1:c.1975C>G | ENSP00000507765.1:p.Arg659Gly | |
| ENST00000321117.10:c.2644C>G MANE Select | ENSP00000324375.5:p.Arg882Gly | |
| ENST00000264709.7:c.2644C>G | ENSP00000264709.3:p.Arg882Gly | |
| ENST00000321117.9:c.2644C>G | ENSP00000324375.5:p.Arg882Gly | |
| ENST00000380746.8:c.2077C>G | ENSP00000370122.4:p.Arg693Gly | |
| ENST00000380756.7:c.*497C>G | ENSP00000370132.3:n.*497C>G | |
| ENST00000402667.1:c.1975C>G | ENSP00000384237.1:p.Arg659Gly | |
| NM_022552.4:c.2644C>G , LRG_459t1:c.2644C>G | NP_072046.2:p.Arg882Gly | |
| NM_153759.3:c.2077C>G , LRG_459t2:c.2077C>G | NP_715640.2:p.Arg693Gly | |
| NM_175629.2:c.2644C>G , LRG_459t4:c.2644C>G | NP_783328.1:p.Arg882Gly | |
| XM_005264175.3:c.2644C>G | XP_005264232.1:p.Arg882Gly | |
| XM_005264177.3:c.1975C>G | XP_005264234.1:p.Arg659Gly | |
| XM_006711958.2:c.2200C>G | XP_006712021.1:p.Arg734Gly | |
| XM_011532662.1:c.2497C>G | XP_011530964.1:p.Arg833Gly | |
| XM_011532663.1:c.2479C>G | XP_011530965.1:p.Arg827Gly | |
| XM_011532665.1:c.2188C>G | XP_011530967.1:p.Arg730Gly | |
| XM_011532666.1:c.2116C>G | XP_011530968.1:p.Arg706Gly | |
| XM_011532667.1:c.1975C>G | XP_011530969.1:p.Arg659Gly | |
| NM_001320893.1:c.2188C>G | NP_001307822.1:p.Arg730Gly | |
| NR_135490.1:n.3181C>G | ||
| XM_005264175.5:c.2644C>G | XP_005264232.1:p.Arg882Gly | |
| XM_005264177.4:c.1975C>G | XP_005264234.1:p.Arg659Gly | |
| XM_011532662.2:c.2497C>G | XP_011530964.1:p.Arg833Gly | |
| XM_011532663.2:c.2479C>G | XP_011530965.1:p.Arg827Gly | |
| XM_011532666.2:c.2116C>G | XP_011530968.1:p.Arg706Gly | |
| XM_011532667.3:c.1975C>G | XP_011530969.1:p.Arg659Gly | |
| XM_017003526.1:c.2644C>G | XP_016859015.1:p.Arg882Gly | |
| XM_017003527.1:c.1975C>G | XP_016859016.1:p.Arg659Gly | |
| XR_001738657.1:n.2851C>G | ||
| NM_001375819.1:c.1975C>G | NP_001362748.1:p.Arg659Gly | |
| NR_135490.2:n.3074C>G | ||
| NM_022552.5:c.2644C>G MANE Select | NP_072046.2:p.Arg882Gly |