Revel Score:
ENST00000330315
0.495
ENST00000542203
0.495
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.138946566G>T , CM000665.2:g.138946566G>T | GRCh38 |
| NC_000003.11:g.138665408G>T , CM000665.1:g.138665408G>T | GRCh37 |
| NC_000003.10:g.140148098G>T | NCBI36 |
| NG_012454.1:g.5575C>A | |
| NG_029796.1:g.4333G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648323.1:c.157C>A MANE Select | ENSP00000497217.1:p.Gln53Lys | |
| ENST00000330315.3:c.157C>A | ENSP00000333188.3:p.Gln53Lys | |
| NM_023067.3:c.157C>A | NP_075555.1:p.Gln53Lys | |
| NM_023067.4:c.157C>A MANE Select | NP_075555.1:p.Gln53Lys |