Revel Score:
ENST00000301415
0.761
ENST00000440075
0.761
ENST00000376970
0.761
ENST00000425460
0.761
ENST00000376965
0.761
ENST00000262269
0.761
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.50259210C>T , CM000681.2:g.50259210C>T | GRCh38 |
| NC_000019.9:g.50762467C>T , CM000681.1:g.50762467C>T | GRCh37 |
| NC_000019.8:g.55454279C>T | NCBI36 |
| NG_011645.1:g.60583C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000425460.6:c.2200C>T | ENSP00000407879.1:p.Arg734Cys | |
| ENST00000642316.2:c.2299C>T MANE Select | ENSP00000493594.1:p.Arg767Cys | |
| ENST00000376970.6:c.2176C>T | ENSP00000366169.3:p.Arg726Cys | |
| ENST00000425460.5:c.2200C>T | ENSP00000407879.1:p.Arg734Cys | |
| ENST00000440075.6:c.-728+9456C>T | ENSP00000406273.3:n.-728+9456C>T | |
| ENST00000596571.5:c.2176C>T | ENSP00000472819.1:p.Arg726Cys | |
| ENST00000598205.5:c.2200C>T | ENSP00000472543.1:p.Arg734Cys | |
| ENST00000599920.5:c.2200C>T | ENSP00000469573.1:p.Arg734Cys | |
| ENST00000601313.5:c.2299C>T | ENSP00000470298.1:p.Arg767Cys | |
| NM_001077186.1:c.2200C>T | NP_001070654.1:p.Arg734Cys | |
| NM_001145809.1:c.2299C>T | NP_001139281.1:p.Arg767Cys | |
| NM_024729.3:c.2176C>T | NP_079005.3:p.Arg726Cys | |
| XM_006723386.2:c.2200C>T | XP_006723449.1:p.Arg734Cys | |
| XM_011527320.1:c.2320C>T | XP_011525622.1:p.Arg774Cys | |
| XM_011527321.1:c.2296C>T | XP_011525623.1:p.Arg766Cys | |
| XM_011527322.1:c.2224C>T | XP_011525624.1:p.Arg742Cys | |
| XM_011527323.1:c.2200C>T | XP_011525625.1:p.Arg734Cys | |
| XM_006723386.4:c.2200C>T | XP_006723449.1:p.Arg734Cys | |
| XM_011527320.2:c.2320C>T | XP_011525622.1:p.Arg774Cys | |
| XM_011527321.2:c.2296C>T | XP_011525623.1:p.Arg766Cys | |
| XM_011527323.2:c.2200C>T | XP_011525625.1:p.Arg734Cys | |
| XM_024451721.1:c.2176C>T | XP_024307489.1:p.Arg726Cys | |
| NM_001077186.2:c.2200C>T | NP_001070654.1:p.Arg734Cys | |
| NM_001145809.2:c.2299C>T MANE Select | NP_001139281.1:p.Arg767Cys | |
| NM_024729.4:c.2176C>T | NP_079005.3:p.Arg726Cys |