Linked Data
ClinVar Variation Id:
261547
dbSNP Id:
rs72817951
ExAC:
10:73483773 G / A
gnomAD v2:
10-73483773-G-A
gnomAD v3:
10-71724016-G-A
gnomAD v4:
10-71724016-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.71724016G>A , CM000672.2:g.71724016G>A | GRCh38 |
| NC_000010.10:g.73483773G>A , CM000672.1:g.73483773G>A | GRCh37 |
| NC_000010.9:g.73153779G>A | NCBI36 |
| NG_008835.1:g.332070G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000224721.12:c.3370-29G>A (CDH23) MANE Select | ENSP00000224721.9:n.3370-29G>A | |
| ENST00000398809.9:c.3374-36G>A (CDH23) | ENSP00000381789.5:n.3374-36G>A | |
| ENST00000224721.10:c.3385-29G>A (CDH23) | ENSP00000224721.8:n.3385-29G>A | |
| ENST00000398786.2:c.-5-7674C>T (C10orf105) | ENSP00000381766.3:n.-5-7674C>T | |
| ENST00000398792.3:n.211-29G>A (CDH23) | ||
| ENST00000398809.8:c.3374-36G>A (CDH23) | ENSP00000381789.5:n.3374-36G>A | |
| ENST00000616684.4:c.3370-29G>A (CDH23) | ENSP00000482036.2:n.3370-29G>A | |
| ENST00000622827.4:c.3370-29G>A (CDH23) | ENSP00000483211.1:n.3370-29G>A | |
| NM_001168390.1:c.-5-7674C>T (C10orf105) | NP_001161862.1:n.-5-7674C>T | |
| NM_001171930.1:c.3370-29G>A (CDH23) | NP_001165401.1:n.3370-29G>A | |
| NM_022124.5:c.3370-29G>A (CDH23) | NP_071407.4:n.3370-29G>A | |
| XM_006717940.2:c.3565-29G>A (CDH23) | XP_006718003.1:n.3565-29G>A | |
| XM_006717942.2:c.3499-29G>A (CDH23) | XP_006718005.1:n.3499-29G>A | |
| XM_011539810.1:c.-6+2391C>T (C10orf105) | XP_011538112.1:n.-6+2391C>T | |
| XM_011540039.1:c.3565-29G>A (CDH23) | XP_011538341.1:n.3565-29G>A | |
| XM_011540040.1:c.3559-29G>A (CDH23) | XP_011538342.1:n.3559-29G>A | |
| XM_011540041.1:c.3505-29G>A (CDH23) | XP_011538343.1:n.3505-29G>A | |
| XM_011540042.1:c.3565-29G>A (CDH23) | XP_011538344.1:n.3565-29G>A | |
| XM_011540043.1:c.3565-29G>A (CDH23) | XP_011538345.1:n.3565-29G>A | |
| XM_011540044.1:c.3430-29G>A (CDH23) | XP_011538346.1:n.3430-29G>A | |
| XM_011540045.1:c.3565-29G>A (CDH23) | XP_011538347.1:n.3565-29G>A | |
| XM_011540046.1:c.3025-29G>A (CDH23) | XP_011538348.1:n.3025-29G>A | |
| XM_011540047.1:c.2383-29G>A (CDH23) | XP_011538349.1:n.2383-29G>A | |
| XM_011540048.1:c.3565-29G>A (CDH23) | XP_011538350.1:n.3565-29G>A | |
| XM_011540049.1:c.3565-29G>A (CDH23) | XP_011538351.1:n.3565-29G>A | |
| XM_011540050.1:c.3565-29G>A (CDH23) | XP_011538352.1:n.3565-29G>A | |
| XM_011540051.1:c.3565-29G>A (CDH23) | XP_011538353.1:n.3565-29G>A | |
| XM_011540052.1:c.-108-29G>A (CDH23) | XP_011538354.1:n.-108-29G>A | |
| XM_011540053.1:c.3565-29G>A (CDH23) | XP_011538355.1:n.3565-29G>A | |
| XR_945796.1:n.3808-29G>A (CDH23) | ||
| NM_001168390.2:c.-5-7674C>T (C10orf105) | NP_001161862.1:n.-5-7674C>T | |
| NM_001171930.2:c.3370-29G>A (CDH23) | NP_001165401.1:n.3370-29G>A | |
| NM_022124.6:c.3370-29G>A (CDH23) MANE Select | NP_071407.4:n.3370-29G>A |