Canonical Allele Identifier: CA16618983
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 422346
ClinVar RCV Id: RCV000480087 RCV001839004
dbSNP Id: rs1064795722
MyVariant Identifiers: chr10:g.73559248G>A (hg19) chr10:g.71799491G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71799491G>A , CM000672.2:g.71799491G>A GRCh38
NC_000010.10:g.73559248G>A , CM000672.1:g.73559248G>A GRCh37
NC_000010.9:g.73229254G>A NCBI36
NG_008835.1:g.407545G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.7225-1G>A MANE Select ENSP00000224721.9:n.7225-1G>A
ENST00000642965.1:c.1158-1G>A ENSP00000495222.1:n.1158-1G>A
ENST00000647092.1:c.822-1G>A ENSP00000495176.1:n.822-1G>A
ENST00000224721.10:c.7240-1G>A ENSP00000224721.8:n.7240-1G>A
ENST00000398788.4:c.505-1G>A ENSP00000381768.3:n.505-1G>A
ENST00000475158.1:n.761-1G>A
ENST00000619887.4:c.505-1G>A ENSP00000478374.1:n.505-1G>A
ENST00000622827.4:c.7225-1G>A ENSP00000483211.1:n.7225-1G>A
NM_001171933.1:c.505-1G>A NP_001165404.1:n.505-1G>A
NM_001171934.1:c.505-1G>A NP_001165405.1:n.505-1G>A
NM_022124.5:c.7225-1G>A NP_071407.4:n.7225-1G>A
XM_006717940.2:c.7420-1G>A XP_006718003.1:n.7420-1G>A
XM_006717942.2:c.7354-1G>A XP_006718005.1:n.7354-1G>A
XM_011540039.1:c.7417-1G>A XP_011538341.1:n.7417-1G>A
XM_011540040.1:c.7414-1G>A XP_011538342.1:n.7414-1G>A
XM_011540041.1:c.7360-1G>A XP_011538343.1:n.7360-1G>A
XM_011540042.1:c.7330-1G>A XP_011538344.1:n.7330-1G>A
XM_011540043.1:c.7420-1G>A XP_011538345.1:n.7420-1G>A
XM_011540044.1:c.7285-1G>A XP_011538346.1:n.7285-1G>A
XM_011540045.1:c.7420-1G>A XP_011538347.1:n.7420-1G>A
XM_011540046.1:c.6880-1G>A XP_011538348.1:n.6880-1G>A
XM_011540047.1:c.6238-1G>A XP_011538349.1:n.6238-1G>A
XM_011540052.1:c.3748-1G>A XP_011538354.1:n.3748-1G>A
NM_022124.6:c.7225-1G>A MANE Select NP_071407.4:n.7225-1G>A
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