Revel Score:
ENST00000398860
0.123
ENST00000398855
0.123
ENST00000224721 (MANE Select)
0.123
ENST00000398792
0.123
gnomAD v2:
gnomAD v3:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.71730595C>G , CM000672.2:g.71730595C>G | GRCh38 |
| NC_000010.10:g.73490352C>G , CM000672.1:g.73490352C>G | GRCh37 |
| NC_000010.9:g.73160358C>G | NCBI36 |
| NG_008835.1:g.338649C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000224721.12:c.3706C>G (CDH23) MANE Select | ENSP00000224721.9:p.Arg1236Gly | |
| ENST00000398809.9:c.3703C>G (CDH23) | ENSP00000381789.5:p.Arg1235Gly | |
| ENST00000224721.10:c.3721C>G (CDH23) | ENSP00000224721.8:p.Arg1241Gly | |
| ENST00000398786.2:c.-6+7133G>C (C10orf105) | ENSP00000381766.3:n.-6+7133G>C | |
| ENST00000398792.3:n.398C>G (CDH23) | ||
| ENST00000398809.8:c.3703C>G (CDH23) | ENSP00000381789.5:p.Arg1235Gly | |
| ENST00000616684.4:c.3706C>G (CDH23) | ENSP00000482036.2:p.Arg1236Gly | |
| ENST00000622827.4:c.3706C>G (CDH23) | ENSP00000483211.1:p.Arg1236Gly | |
| NM_001168390.1:c.-6+7133G>C (C10orf105) | NP_001161862.1:n.-6+7133G>C | |
| NM_001171930.1:c.3706C>G (CDH23) | NP_001165401.1:p.Arg1236Gly | |
| NM_022124.5:c.3706C>G (CDH23) | NP_071407.4:p.Arg1236Gly | |
| XM_006717940.2:c.3901C>G (CDH23) | XP_006718003.1:p.Arg1301Gly | |
| XM_006717942.2:c.3835C>G (CDH23) | XP_006718005.1:p.Arg1279Gly | |
| XM_011540039.1:c.3901C>G (CDH23) | XP_011538341.1:p.Arg1301Gly | |
| XM_011540040.1:c.3895C>G (CDH23) | XP_011538342.1:p.Arg1299Gly | |
| XM_011540041.1:c.3841C>G (CDH23) | XP_011538343.1:p.Arg1281Gly | |
| XM_011540042.1:c.3901C>G (CDH23) | XP_011538344.1:p.Arg1301Gly | |
| XM_011540043.1:c.3901C>G (CDH23) | XP_011538345.1:p.Arg1301Gly | |
| XM_011540044.1:c.3766C>G (CDH23) | XP_011538346.1:p.Arg1256Gly | |
| XM_011540045.1:c.3901C>G (CDH23) | XP_011538347.1:p.Arg1301Gly | |
| XM_011540046.1:c.3361C>G (CDH23) | XP_011538348.1:p.Arg1121Gly | |
| XM_011540047.1:c.2719C>G (CDH23) | XP_011538349.1:p.Arg907Gly | |
| XM_011540048.1:c.3901C>G (CDH23) | XP_011538350.1:p.Arg1301Gly | |
| XM_011540049.1:c.3901C>G (CDH23) | XP_011538351.1:p.Arg1301Gly | |
| XM_011540050.1:c.3901C>G (CDH23) | XP_011538352.1:p.Arg1301Gly | |
| XM_011540051.1:c.3901C>G (CDH23) | XP_011538353.1:p.Arg1301Gly | |
| XM_011540052.1:c.229C>G (CDH23) | XP_011538354.1:p.Arg77Gly | |
| XM_011540053.1:c.3901C>G (CDH23) | XP_011538355.1:p.Arg1301Gly | |
| XR_945796.1:n.4144C>G (CDH23) | ||
| NM_001168390.2:c.-6+7133G>C (C10orf105) | NP_001161862.1:n.-6+7133G>C | |
| NM_001171930.2:c.3706C>G (CDH23) | NP_001165401.1:p.Arg1236Gly | |
| NM_022124.6:c.3706C>G (CDH23) MANE Select | NP_071407.4:p.Arg1236Gly |