Revel Score:
ENST00000286479 (MANE Select)
0.114
ENST00000520116
0.114
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.18400533A>C , CM000670.2:g.18400533A>C | GRCh38 |
| NC_000008.10:g.18258043A>C , CM000670.1:g.18258043A>C | GRCh37 |
| NC_000008.9:g.18302323A>C | NCBI36 |
| NG_012246.1:g.14289A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286479.4:c.530A>C MANE Select | ENSP00000286479.3:p.Asn177Thr | |
| ENST00000286479.3:c.530A>C | ENSP00000286479.3:p.Asn177Thr | |
| ENST00000520116.1:c.140A>C | ENSP00000428416.1:p.Asn47Thr | |
| NM_000015.2:c.530A>C | NP_000006.2:p.Asn177Thr | |
| XM_011544358.1:c.530A>C | XP_011542660.1:p.Asn177Thr | |
| XM_017012938.1:c.530A>C | XP_016868427.1:p.Asn177Thr | |
| NM_000015.3:c.530A>C MANE Select | NP_000006.2:p.Asn177Thr |