Revel Score:
ENST00000395925 (MANE Select)
0.126
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00165484 (MID)
Genomes Max Group AF
0.00065547 (AMR)
Exomes Max Group AF
0.00160249 (MID)
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.41965138A>C , CM000669.2:g.41965138A>C | GRCh38 |
| NC_000007.13:g.42004736A>C , CM000669.1:g.42004736A>C | GRCh37 |
| NC_000007.12:g.41971261A>C | NCBI36 |
| NG_008434.1:g.276883T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395925.8:c.3935T>G MANE Select | ENSP00000379258.3:p.Met1312Arg | |
| ENST00000677288.1:c.3761T>G | ENSP00000503986.1:p.Met1254Arg | |
| ENST00000677605.1:c.3935T>G | ENSP00000503743.1:p.Met1312Arg | |
| ENST00000678429.1:c.3935T>G | ENSP00000502957.1:p.Met1312Arg | |
| ENST00000395925.7:c.3935T>G | ENSP00000379258.3:p.Met1312Arg | |
| ENST00000479210.1:n.3912T>G | ||
| NM_000168.5:c.3935T>G | NP_000159.3:p.Met1312Arg | |
| XM_005249703.1:c.3935T>G | XP_005249760.1:p.Met1312Arg | |
| XM_005249704.2:c.3935T>G | XP_005249761.1:p.Met1312Arg | |
| XM_011515272.1:c.3935T>G | XP_011513574.1:p.Met1312Arg | |
| XM_011515273.1:c.3935T>G | XP_011513575.1:p.Met1312Arg | |
| XM_011515274.1:c.3758T>G | XP_011513576.1:p.Met1253Arg | |
| XM_011515274.2:c.3758T>G | XP_011513576.1:p.Met1253Arg | |
| XM_017011997.1:c.3932T>G | XP_016867486.1:p.Met1311Arg | |
| NM_000168.6:c.3935T>G MANE Select | NP_000159.3:p.Met1312Arg |