Revel Score:
ENST00000348749 (MANE Select)
0.580
ENST00000261007
0.580
ENST00000409542
0.580
ENST00000409219
0.580
ENST00000409323
0.580
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.174753570G>T , CM000664.2:g.174753570G>T | GRCh38 |
| NC_000002.11:g.175618298G>T , CM000664.1:g.175618298G>T | GRCh37 |
| NC_000002.10:g.175326544G>T | NCBI36 |
| NG_008172.1:g.15903C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000636168.2:c.222C>A | ENSP00000490338.2:p.Asn74Lys | |
| ENST00000672640.1:c.222C>A | ENSP00000500507.1:p.Asn74Lys | |
| ENST00000261007.9:c.786C>A | ENSP00000261007.5:p.Asn262Lys | |
| ENST00000348749.9:c.711C>A MANE Select | ENSP00000261008.5:p.Asn237Lys | |
| ENST00000409219.5:c.711C>A | ENSP00000386611.1:p.Asn237Lys | |
| ENST00000409323.1:c.711C>A | ENSP00000386684.1:p.Asn237Lys | |
| ENST00000409542.5:c.465C>A | ENSP00000387026.1:p.Asn155Lys | |
| ENST00000435083.5:c.*355C>A | ENSP00000395805.1:n.*355C>A | |
| NM_000079.3:c.711C>A | NP_000070.1:p.Asn237Lys | |
| NM_001039523.2:c.786C>A | NP_001034612.1:p.Asn262Lys | |
| XM_017003256.1:c.807C>A | XP_016858745.1:p.Asn269Lys | |
| XM_017003257.1:c.732C>A | XP_016858746.1:p.Asn244Lys | |
| NM_000079.4:c.711C>A MANE Select | NP_000070.1:p.Asn237Lys | |
| NM_001039523.3:c.786C>A | NP_001034612.1:p.Asn262Lys |