Revel Score:
ENST00000249760
0.528
ENST00000479013
0.528
ENST00000487418 (MANE Select)
0.528
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.40405828A>C , CM000677.2:g.40405828A>C | GRCh38 |
| NC_000015.9:g.40698029A>C , CM000677.1:g.40698029A>C | GRCh37 |
| NC_000015.8:g.38485321A>C | NCBI36 |
| NG_011986.1:g.5344A>C | |
| NG_011986.2:g.5344A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000479013.7:c.1A>C | ENSP00000417990.3:p.Met1Leu | |
| ENST00000487418.8:c.1A>C MANE Select | ENSP00000418397.3:p.Met1Leu | |
| ENST00000610693.5:c.1A>C | ENSP00000479359.2:p.Met1Leu | |
| ENST00000650656.1:c.10A>C | ENSP00000498731.1:p.Met4Leu | |
| ENST00000651168.1:c.10A>C | ENSP00000499074.1:p.Met4Leu | |
| ENST00000479013.6:c.10A>C | ENSP00000417990.2:p.Met4Leu | |
| ENST00000487418.6:c.10A>C | ENSP00000418397.2:p.Met4Leu | |
| ENST00000610693.4:c.10A>C | ENSP00000479359.1:p.Met4Leu | |
| NM_001159508.1:c.10A>C | NP_001152980.1:p.Met4Leu | |
| NM_002225.3:c.10A>C | NP_002216.2:p.Met4Leu | |
| XM_005254350.2:c.10A>C | XP_005254407.1:p.Met4Leu | |
| XM_005254356.2:c.10A>C | XP_005254413.1:p.Met4Leu | |
| XM_006720492.2:c.10A>C | XP_006720555.1:p.Met4Leu | |
| XM_006720493.2:c.10A>C | XP_006720556.1:p.Met4Leu | |
| XM_006720494.2:c.10A>C | XP_006720557.1:p.Met4Leu | |
| XM_006720495.2:c.10A>C | XP_006720558.1:p.Met4Leu | |
| XM_011521523.1:c.10A>C | XP_011519825.1:p.Met4Leu | |
| XM_011521524.1:c.10A>C | XP_011519826.1:p.Met4Leu | |
| XR_243097.3:n.10A>C | ||
| XR_243098.2:n.10A>C | ||
| XR_429453.2:n.111A>C | ||
| NM_001159508.2:c.1A>C | NP_001152980.2:p.Met1Leu | |
| NM_001354597.2:c.-427A>C | NP_001341526.1:n.-427A>C | |
| NM_001354598.2:c.1A>C | NP_001341527.2:p.Met1Leu | |
| NM_001354599.2:c.1A>C | NP_001341528.2:p.Met1Leu | |
| NM_001354600.2:c.1A>C | NP_001341529.2:p.Met1Leu | |
| NM_001354601.2:c.1A>C | NP_001341530.2:p.Met1Leu | |
| NM_002225.4:c.1A>C | NP_002216.3:p.Met1Leu | |
| NR_148925.1:n.32A>C | ||
| XM_006720495.3:c.10A>C | XP_006720558.1:p.Met4Leu | |
| XM_017022149.1:c.10A>C | XP_016877638.1:p.Met4Leu | |
| XM_017022150.1:c.10A>C | XP_016877639.1:p.Met4Leu | |
| XM_017022153.1:c.10A>C | XP_016877642.1:p.Met4Leu | |
| XM_017022155.2:c.10A>C | XP_016877644.1:p.Met4Leu | |
| XM_017022157.1:c.10A>C | XP_016877646.1:p.Met4Leu | |
| XM_017022158.2:c.10A>C | XP_016877647.1:p.Met4Leu | |
| XR_001751264.1:n.22A>C | ||
| NM_001159508.3:c.1A>C | NP_001152980.2:p.Met1Leu | |
| NM_001354597.3:c.-427A>C | NP_001341526.1:n.-427A>C | |
| NM_001354598.3:c.1A>C | NP_001341527.2:p.Met1Leu | |
| NM_001354599.3:c.1A>C | NP_001341528.2:p.Met1Leu | |
| NM_001354600.3:c.1A>C | NP_001341529.2:p.Met1Leu | |
| NM_001354601.3:c.1A>C | NP_001341530.2:p.Met1Leu | |
| NM_002225.5:c.1A>C MANE Select | NP_002216.3:p.Met1Leu | |
| NR_148925.2:n.34A>C |