Revel Score:
ENST00000441560
0.620
ENST00000358385 (MANE Select)
0.620
ENST00000357032
0.620
ENST00000354525
0.620
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50614422A>T , CM000676.2:g.50614422A>T | GRCh38 |
| NC_000014.8:g.51081140A>T , CM000676.1:g.51081140A>T | GRCh37 |
| NC_000014.7:g.50150890A>T | NCBI36 |
| NG_009028.1:g.86341A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553509.2:c.773A>T | ENSP00000450989.2:p.His258Leu | |
| ENST00000556478.3:c.773A>T | ENSP00000501428.2:p.His258Leu | |
| ENST00000682037.1:c.773A>T | ENSP00000508289.1:p.His258Leu | |
| ENST00000682219.1:n.2111A>T | ||
| ENST00000682487.1:n.1107A>T | ||
| ENST00000683037.1:n.694A>T | ||
| ENST00000683330.1:n.1107A>T | ||
| ENST00000683837.1:n.1107A>T | ||
| ENST00000358385.12:c.773A>T MANE Select | ENSP00000351155.7:p.His258Leu | |
| ENST00000674288.1:c.*2065A>T | ENSP00000501522.1:n.*2065A>T | |
| ENST00000358385.10:c.773A>T | ENSP00000351155.6:p.His258Leu | |
| ENST00000441560.6:c.773A>T | ENSP00000413675.2:p.His258Leu | |
| ENST00000555266.1:c.44A>T | ENSP00000450897.1:p.His15Leu | |
| NM_001127713.1:c.773A>T | NP_001121185.1:p.His258Leu | |
| NM_015915.4:c.773A>T | NP_056999.2:p.His258Leu | |
| NM_181598.3:c.773A>T | NP_853629.2:p.His258Leu | |
| NM_015915.5:c.773A>T MANE Select | NP_056999.2:p.His258Leu | |
| NM_181598.4:c.773A>T | NP_853629.2:p.His258Leu |