Canonical Allele Identifier: CA5546932

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71811507G>A , CM000672.2:g.71811507G>A	GRCh38
NC_000010.10:g.73571264G>A , CM000672.1:g.73571264G>A	GRCh37
NC_000010.9:g.73241270G>A	NCBI36
NG_008835.1:g.419561G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_022124.6:c.9199-4G>A MANE Select	NP_071407.4:n.9199-4G>A
ENST00000224721.12:c.9199-4G>A MANE Select	ENSP00000224721.9:n.9199-4G>A
NM_001171933.1:c.2479-4G>A	NP_001165404.1:n.2479-4G>A
NM_001171934.1:c.2479-4G>A	NP_001165405.1:n.2479-4G>A
NM_022124.5:c.9199-4G>A	NP_071407.4:n.9199-4G>A
ENST00000224721.10:c.9214-4G>A	ENSP00000224721.8:n.9214-4G>A
ENST00000398788.4:c.2479-4G>A	ENSP00000381768.3:n.2479-4G>A
ENST00000475158.1:n.2735-4G>A
ENST00000619887.4:c.2479-4G>A	ENSP00000478374.1:n.2479-4G>A
ENST00000622827.4:c.9199-4G>A	ENSP00000483211.1:n.9199-4G>A
ENST00000642965.1:c.3132-4G>A	ENSP00000495222.1:n.3132-4G>A
ENST00000647092.1:c.2796-4G>A	ENSP00000495176.1:n.2796-4G>A
XM_006717940.2:c.9394-4G>A	XP_006718003.1:n.9394-4G>A
XM_006717942.2:c.9328-4G>A	XP_006718005.1:n.9328-4G>A
XM_011540039.1:c.9391-4G>A	XP_011538341.1:n.9391-4G>A
XM_011540040.1:c.9388-4G>A	XP_011538342.1:n.9388-4G>A
XM_011540041.1:c.9334-4G>A	XP_011538343.1:n.9334-4G>A
XM_011540042.1:c.9304-4G>A	XP_011538344.1:n.9304-4G>A
XM_011540043.1:c.9394-4G>A	XP_011538345.1:n.9394-4G>A
XM_011540044.1:c.9259-4G>A	XP_011538346.1:n.9259-4G>A
XM_011540045.1:c.9394-4G>A	XP_011538347.1:n.9394-4G>A
XM_011540046.1:c.8854-4G>A	XP_011538348.1:n.8854-4G>A
XM_011540047.1:c.8212-4G>A	XP_011538349.1:n.8212-4G>A
XM_011540052.1:c.5722-4G>A	XP_011538354.1:n.5722-4G>A