Canonical Allele Identifier: CA2574456132

Gene: CDH23

Linked Data

• gnomAD v4: 10-71799455-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71799455C>G , CM000672.2:g.71799455C>G	GRCh38
NC_000010.10:g.73559212C>G , CM000672.1:g.73559212C>G	GRCh37
NC_000010.9:g.73229218C>G	NCBI36
NG_008835.1:g.407509C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7225-37C>G MANE Select	ENSP00000224721.9:n.7225-37C>G
ENST00000642965.1:c.1158-37C>G	ENSP00000495222.1:n.1158-37C>G
ENST00000647092.1:c.822-37C>G	ENSP00000495176.1:n.822-37C>G
ENST00000224721.10:c.7240-37C>G	ENSP00000224721.8:n.7240-37C>G
ENST00000398788.4:c.505-37C>G	ENSP00000381768.3:n.505-37C>G
ENST00000475158.1:n.761-37C>G
ENST00000619887.4:c.505-37C>G	ENSP00000478374.1:n.505-37C>G
ENST00000622827.4:c.7225-37C>G	ENSP00000483211.1:n.7225-37C>G
NM_001171933.1:c.505-37C>G	NP_001165404.1:n.505-37C>G
NM_001171934.1:c.505-37C>G	NP_001165405.1:n.505-37C>G
NM_022124.5:c.7225-37C>G	NP_071407.4:n.7225-37C>G
XM_006717940.2:c.7420-37C>G	XP_006718003.1:n.7420-37C>G
XM_006717942.2:c.7354-37C>G	XP_006718005.1:n.7354-37C>G
XM_011540039.1:c.7417-37C>G	XP_011538341.1:n.7417-37C>G
XM_011540040.1:c.7414-37C>G	XP_011538342.1:n.7414-37C>G
XM_011540041.1:c.7360-37C>G	XP_011538343.1:n.7360-37C>G
XM_011540042.1:c.7330-37C>G	XP_011538344.1:n.7330-37C>G
XM_011540043.1:c.7420-37C>G	XP_011538345.1:n.7420-37C>G
XM_011540044.1:c.7285-37C>G	XP_011538346.1:n.7285-37C>G
XM_011540045.1:c.7420-37C>G	XP_011538347.1:n.7420-37C>G
XM_011540046.1:c.6880-37C>G	XP_011538348.1:n.6880-37C>G
XM_011540047.1:c.6238-37C>G	XP_011538349.1:n.6238-37C>G
XM_011540052.1:c.3748-37C>G	XP_011538354.1:n.3748-37C>G
NM_022124.6:c.7225-37C>G MANE Select	NP_071407.4:n.7225-37C>G