Revel Score:
ENST00000540563
0.910
ENST00000545496
0.910
ENST00000381134 (MANE Select)
0.910
ENST00000438544
0.910
gnomAD v3:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.2953163C>A , CM000685.2:g.2953163C>A | GRCh38 |
| NC_000023.10:g.2871204C>A , CM000685.1:g.2871204C>A | GRCh37 |
| NC_000023.9:g.2881204C>A | NCBI36 |
| NG_007091.1:g.16108G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000483425.2:n.495G>T | ||
| ENST00000540563.6:c.410G>T | ENSP00000438198.2:p.Gly137Val | |
| ENST00000681960.1:n.736G>T | ||
| ENST00000681963.1:c.485G>T | ENSP00000507760.1:p.Gly162Val | |
| ENST00000682184.1:c.307+2253G>T | ENSP00000507043.1:n.307+2253G>T | |
| ENST00000682364.1:c.410G>T | ENSP00000507604.1:p.Gly137Val | |
| ENST00000682745.1:n.495G>T | ||
| ENST00000683071.1:n.302G>T | ||
| ENST00000683191.1:n.190G>T | ||
| ENST00000683290.1:c.485G>T | ENSP00000508156.1:p.Gly162Val | |
| ENST00000683677.1:c.398G>T | ENSP00000506786.1:p.Gly133Val | |
| ENST00000683854.1:n.495G>T | ||
| ENST00000683958.1:c.410G>T | ENSP00000507756.1:p.Gly137Val | |
| ENST00000684045.1:n.724G>T | ||
| ENST00000684077.1:c.248G>T | ENSP00000506767.1:p.Gly83Val | |
| ENST00000684117.1:c.248G>T | ENSP00000508337.1:p.Gly83Val | |
| ENST00000684364.1:c.398G>T | ENSP00000507304.1:p.Gly133Val | |
| ENST00000684687.1:c.248G>T | ENSP00000507266.1:p.Gly83Val | |
| ENST00000684738.1:c.410G>T | ENSP00000507481.1:p.Gly137Val | |
| ENST00000381134.9:c.410G>T MANE Select | ENSP00000370526.3:p.Gly137Val | |
| ENST00000545496.6:c.485G>T | ENSP00000441417.1:p.Gly162Val | |
| ENST00000672027.1:c.485G>T | ENSP00000500220.1:p.Gly162Val | |
| ENST00000672097.1:c.410G>T | ENSP00000500727.1:p.Gly137Val | |
| ENST00000672606.1:c.410G>T | ENSP00000500638.1:p.Gly137Val | |
| ENST00000672761.1:c.248G>T | ENSP00000500108.1:p.Gly83Val | |
| ENST00000673032.1:c.248G>T | ENSP00000500778.1:p.Gly83Val | |
| ENST00000381134.7:c.410G>T | ENSP00000370526.3:p.Gly137Val | |
| ENST00000438544.5:c.410G>T | ENSP00000406528.1:p.Gly137Val | |
| ENST00000483425.1:n.66G>T | ||
| ENST00000540563.5:c.275G>T | ENSP00000438198.1:p.Gly92Val | |
| ENST00000545496.5:c.485G>T | ENSP00000441417.1:p.Gly162Val | |
| NM_000047.2:c.410G>T | NP_000038.2:p.Gly137Val | |
| NM_001282628.1:c.485G>T | NP_001269557.1:p.Gly162Val | |
| NM_001282631.1:c.275G>T | NP_001269560.1:p.Gly92Val | |
| XM_005274518.2:c.437G>T | XP_005274575.1:p.Gly146Val | |
| XM_005274519.3:c.410G>T | XP_005274576.1:p.Gly137Val | |
| XM_005274521.3:c.248G>T | XP_005274578.1:p.Gly83Val | |
| XM_011545519.1:c.248G>T | XP_011543821.1:p.Gly83Val | |
| XM_011545520.1:c.485G>T | XP_011543822.1:p.Gly162Val | |
| XM_011545521.1:c.410G>T | XP_011543823.1:p.Gly137Val | |
| XM_005274519.4:c.410G>T | XP_005274576.1:p.Gly137Val | |
| XM_005274521.4:c.248G>T | XP_005274578.1:p.Gly83Val | |
| XM_017029525.1:c.485G>T | XP_016885014.1:p.Gly162Val | |
| XM_017029526.1:c.485G>T | XP_016885015.1:p.Gly162Val | |
| NM_000047.3:c.410G>T MANE Select | NP_000038.2:p.Gly137Val | |
| NM_001282631.2:c.248G>T | NP_001269560.2:p.Gly83Val | |
| NM_001369079.1:c.437G>T | NP_001356008.1:p.Gly146Val | |
| NM_001369080.1:c.485G>T | NP_001356009.1:p.Gly162Val | |
| NM_001282628.2:c.485G>T | NP_001269557.1:p.Gly162Val |