Revel Score:
ENST00000300851
0.862
ENST00000319788
0.862
ENST00000354895
0.862
ENST00000394975 (MANE Select)
0.862
ENST00000529564
0.862
gnomAD v2:
gnomAD v3:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.31094645C>A , CM000678.2:g.31094645C>A | GRCh38 |
| NC_000016.9:g.31105966C>A , CM000678.1:g.31105966C>A | GRCh37 |
| NC_000016.8:g.31013467C>A | NCBI36 |
| NG_011564.1:g.5311G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000394975.3:c.85G>T MANE Select | ENSP00000378426.2:p.Val29Leu | |
| ENST00000300851.10:c.85G>T | ENSP00000300851.6:p.Val29Leu | |
| ENST00000319788.11:c.85G>T | ENSP00000326135.7:p.Val29Leu | |
| ENST00000354895.4:c.85G>T | ENSP00000346969.4:p.Val29Leu | |
| ENST00000394975.2:c.85G>T | ENSP00000378426.2:p.Val29Leu | |
| ENST00000420057.2:c.245+744G>T | ||
| ENST00000498155.1:c.270+744G>T | ENSP00000417662.1:n.270+744G>T | |
| ENST00000529564.1:c.85G>T | ENSP00000431371.1:p.Val29Leu | |
| ENST00000532364.1:c.85G>T | ENSP00000460316.1:p.Val29Leu | |
| NM_001311311.1:c.85G>T | NP_001298240.1:p.Val29Leu | |
| NM_024006.4:c.85G>T | NP_076869.1:p.Val29Leu | |
| NM_024006.5:c.85G>T | NP_076869.1:p.Val29Leu | |
| NM_206824.1:c.85G>T | NP_996560.1:p.Val29Leu | |
| NM_206824.2:c.85G>T | NP_996560.1:p.Val29Leu | |
| XM_011545944.1:c.85G>T | XP_011544246.1:p.Val29Leu | |
| XM_011545945.1:c.85G>T | XP_011544247.1:p.Val29Leu | |
| XR_950848.1:n.873G>T | ||
| NM_024006.6:c.85G>T MANE Select | NP_076869.1:p.Val29Leu | |
| NM_001311311.2:c.85G>T | NP_001298240.1:p.Val29Leu | |
| NM_206824.3:c.85G>T | NP_996560.1:p.Val29Leu |