Revel Score:
ENST00000272895 (MANE Select)
0.692
ENST00000389661
0.692
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.215011451G>A , CM000664.2:g.215011451G>A | GRCh38 |
| NC_000002.11:g.215876175G>A , CM000664.1:g.215876175G>A | GRCh37 |
| NC_000002.10:g.215584420G>A | NCBI36 |
| NG_007074.1:g.131977C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272895.12:c.2320C>T MANE Select | ENSP00000272895.7:p.Pro774Ser | |
| ENST00000272895.11:c.2320C>T | ENSP00000272895.7:p.Pro774Ser | |
| ENST00000389661.4:c.1366C>T | ENSP00000374312.4:p.Pro456Ser | |
| NM_015657.3:c.1366C>T | NP_056472.2:p.Pro456Ser | |
| NM_173076.2:c.2320C>T | NP_775099.2:p.Pro774Ser | |
| NR_103740.1:n.2564C>T | ||
| XM_011510951.1:c.2320C>T | XP_011509253.1:p.Pro774Ser | |
| XM_011510952.1:c.2320C>T | XP_011509254.1:p.Pro774Ser | |
| XM_011510951.2:c.2320C>T | XP_011509253.1:p.Pro774Ser | |
| NM_173076.3:c.2320C>T MANE Select | NP_775099.2:p.Pro774Ser | |
| NR_103740.2:n.2762C>T | ||
| NM_015657.4:c.1366C>T | NP_056472.2:p.Pro456Ser |