Revel Score:
ENST00000295550 (MANE Select)
0.988
ENST00000347401
0.988
ENST00000353578
0.988
ENST00000472056
0.988
ENST00000409809
0.988
ENST00000346358
0.988
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.237361156C>A , CM000664.2:g.237361156C>A | GRCh38 |
| NC_000002.11:g.238269799C>A , CM000664.1:g.238269799C>A | GRCh37 |
| NC_000002.10:g.237934538C>A | NCBI36 |
| NG_008676.1:g.58052G>T , LRG_473:g.58052G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000353578.9:c.5557G>T | ENSP00000315873.4:p.Gly1853Cys | |
| ENST00000295550.9:c.6175G>T MANE Select | ENSP00000295550.4:p.Gly2059Cys | |
| ENST00000295550.8:c.6175G>T | ENSP00000295550.4:p.Gly2059Cys | |
| ENST00000347401.7:c.4354G>T | ENSP00000315609.4:p.Gly1452Cys | |
| ENST00000353578.8:c.5557G>T | ENSP00000315873.4:p.Gly1853Cys | |
| ENST00000409809.5:c.5557G>T | ENSP00000386844.1:p.Gly1853Cys | |
| ENST00000472056.5:c.4354G>T | ENSP00000418285.1:p.Gly1452Cys | |
| NM_004369.3:c.6175G>T , LRG_473t1:c.6175G>T | NP_004360.2:p.Gly2059Cys | |
| NM_057166.4:c.4354G>T | NP_476507.3:p.Gly1452Cys | |
| NM_057167.3:c.5557G>T | NP_476508.2:p.Gly1853Cys | |
| XM_005246065.1:c.5575G>T | XP_005246122.1:p.Gly1859Cys | |
| XM_005246066.1:c.4954G>T | XP_005246123.1:p.Gly1652Cys | |
| XM_006712253.1:c.5674G>T | XP_006712316.1:p.Gly1892Cys | |
| XM_011510574.1:c.6172G>T | XP_011508876.1:p.Gly2058Cys | |
| XM_011510575.1:c.3769G>T | XP_011508877.1:p.Gly1257Cys | |
| XM_017003304.1:c.3769G>T | XP_016858793.1:p.Gly1257Cys | |
| XM_024452684.1:c.4954G>T | XP_024308452.1:p.Gly1652Cys | |
| NM_004369.4:c.6175G>T MANE Select | NP_004360.2:p.Gly2059Cys | |
| NM_057166.5:c.4354G>T | NP_476507.3:p.Gly1452Cys | |
| NM_057167.4:c.5557G>T | NP_476508.2:p.Gly1853Cys |