Revel Score:
ENST00000295754 (MANE Select)
0.898
ENST00000359013
0.898
ENST00000439925
0.898
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.30672334A>G , CM000665.2:g.30672334A>G | GRCh38 |
| NC_000003.11:g.30713826A>G , CM000665.1:g.30713826A>G | GRCh37 |
| NC_000003.10:g.30688830A>G | NCBI36 |
| NG_007490.1:g.70833A>G , LRG_779:g.70833A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295754.10:c.1151A>G MANE Select | ENSP00000295754.5:p.Asn384Ser | |
| ENST00000672866.1:n.2747A>G | ||
| ENST00000295754.9:c.1151A>G | ENSP00000295754.5:p.Asn384Ser | |
| ENST00000359013.4:c.1226A>G | ENSP00000351905.4:p.Asn409Ser | |
| NM_001024847.2:c.1226A>G , LRG_779t1:c.1226A>G | NP_001020018.1:p.Asn409Ser | |
| NM_003242.5:c.1151A>G | NP_003233.4:p.Asn384Ser | |
| XM_011534043.1:c.1178A>G | XP_011532345.1:p.Asn393Ser | |
| XM_011534044.1:c.1103A>G | XP_011532346.1:p.Asn368Ser | |
| XM_011534045.1:c.1046A>G | XP_011532347.1:p.Asn349Ser | |
| XM_011534043.2:c.1178A>G | XP_011532345.1:p.Asn393Ser | |
| XM_011534045.3:c.1046A>G | XP_011532347.1:p.Asn349Ser | |
| XM_017007106.1:c.1046A>G | XP_016862595.1:p.Asn349Ser | |
| NM_003242.6:c.1151A>G MANE Select | NP_003233.4:p.Asn384Ser |