Revel Score:
ENST00000218099 (MANE Select)
0.992
ENST00000394090
0.992
gnomAD v2:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.139561925C>T , CM000685.2:g.139561925C>T | GRCh38 |
| NC_000023.10:g.138644084C>T , CM000685.1:g.138644084C>T | GRCh37 |
| NC_000023.9:g.138471750C>T | NCBI36 |
| NG_007994.1:g.36190C>T , LRG_556:g.36190C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218099.7:c.1240C>T MANE Select | ENSP00000218099.2:p.Pro414Ser | |
| ENST00000643157.1:n.1723+184C>T | ||
| ENST00000218099.6:c.1240C>T | ENSP00000218099.2:p.Pro414Ser | |
| ENST00000394090.2:c.1126C>T | ENSP00000377650.2:p.Pro376Ser | |
| NM_000133.3:c.1240C>T , LRG_556t1:c.1240C>T | NP_000124.1:p.Pro414Ser | |
| NM_001313913.1:c.1126C>T | NP_001300842.1:p.Pro376Ser | |
| XM_005262397.3:c.1111C>T | XP_005262454.1:p.Pro371Ser | |
| XM_005262397.4:c.1111C>T | XP_005262454.1:p.Pro371Ser | |
| NM_000133.4:c.1240C>T MANE Select | NP_000124.1:p.Pro414Ser | |
| NM_001313913.2:c.1126C>T | NP_001300842.1:p.Pro376Ser |