This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Revel Score:
ENST00000360256 (MANE Select)
0.904
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154966098C>G , CM000685.2:g.154966098C>G | GRCh38 |
| NC_000023.10:g.154194373C>G , CM000685.1:g.154194373C>G | GRCh37 |
| NC_000023.9:g.153847567C>G | NCBI36 |
| NG_011403.1:g.61626G>C | |
| NG_011403.2:g.61626G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.1315G>C MANE Select | ENSP00000353393.4:p.Gly439Arg | |
| ENST00000647125.1:c.*1191G>C | ENSP00000496062.1:n.*1191G>C | |
| ENST00000360256.8:c.1315G>C | ENSP00000353393.4:p.Gly439Arg | |
| ENST00000483822.2:n.135G>C | ||
| NM_000132.3:c.1315G>C | NP_000123.1:p.Gly439Arg | |
| XM_011531126.1:c.1210G>C | XP_011529428.1:p.Gly404Arg | |
| NM_000132.4:c.1315G>C MANE Select | NP_000123.1:p.Gly439Arg |