Revel Score:
ENST00000553106 (MANE Select)
0.406
ENST00000307000
0.406
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102866605T>G , CM000674.2:g.102866605T>G | GRCh38 |
| NC_000012.11:g.103260383T>G , CM000674.1:g.103260383T>G | GRCh37 |
| NC_000012.10:g.101784513T>G | NCBI36 |
| NG_008690.1:g.55998A>C | |
| NG_008690.2:g.96806A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.500A>C MANE Select | ENSP00000448059.1:p.Asn167Thr | |
| ENST00000307000.7:c.485A>C | ENSP00000303500.2:p.Asn162Thr | |
| ENST00000549111.5:n.596A>C | ||
| ENST00000551988.5:n.530+10857A>C | ||
| ENST00000553106.5:c.500A>C | ENSP00000448059.1:p.Asn167Thr | |
| NM_000277.1:c.500A>C | NP_000268.1:p.Asn167Thr | |
| XM_011538422.1:c.500A>C | XP_011536724.1:p.Asn167Thr | |
| NM_000277.2:c.500A>C | NP_000268.1:p.Asn167Thr | |
| NM_001354304.1:c.500A>C | NP_001341233.1:p.Asn167Thr | |
| XM_017019370.2:c.500A>C | XP_016874859.1:p.Asn167Thr | |
| NM_000277.3:c.500A>C MANE Select | NP_000268.1:p.Asn167Thr | |
| NM_001354304.2:c.500A>C | NP_001341233.1:p.Asn167Thr |