Revel Score:
ENST00000496887
0.975
ENST00000155840 (MANE Select)
0.975
ENST00000335475
0.975
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2572081T>C , CM000673.2:g.2572081T>C | GRCh38 |
| NC_000011.9:g.2593311T>C , CM000673.1:g.2593311T>C | GRCh37 |
| NC_000011.8:g.2549887T>C | NCBI36 |
| NG_008935.1:g.132091T>C , LRG_287:g.132091T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496887.7:c.491T>C | ENSP00000434560.2:p.Leu164Pro | |
| ENST00000646564.2:c.478-11354T>C | ENSP00000495806.2:n.478-11354T>C | |
| ENST00000155840.12:c.752T>C MANE Select | ENSP00000155840.2:p.Leu251Pro | |
| ENST00000335475.6:c.371T>C | ENSP00000334497.5:p.Leu124Pro | |
| ENST00000646564.1:c.124-11354T>C | ENSP00000495806.1:n.124-11354T>C | |
| ENST00000155840.9:c.752T>C | ENSP00000155840.2:p.Leu251Pro | |
| ENST00000335475.5:c.371T>C | ENSP00000334497.5:p.Leu124Pro | |
| ENST00000496887.6:c.491T>C | ENSP00000434560.1:p.Leu164Pro | |
| NM_000218.2:c.752T>C , LRG_287t1:c.752T>C | NP_000209.2:p.Leu251Pro | |
| NM_181798.1:c.371T>C , LRG_287t2:c.371T>C | NP_861463.1:p.Leu124Pro | |
| NM_000218.3:c.752T>C MANE Select | NP_000209.2:p.Leu251Pro |