Canonical Allele Identifier: CA5547141

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71812904G>A , CM000672.2:g.71812904G>A	GRCh38
NC_000010.10:g.73572661G>A , CM000672.1:g.73572661G>A	GRCh37
NC_000010.9:g.73242667G>A	NCBI36
NG_008835.1:g.420958G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_022124.6:c.9633+14G>A MANE Select	NP_071407.4:n.9633+14G>A
ENST00000224721.12:c.9633+14G>A MANE Select	ENSP00000224721.9:n.9633+14G>A
NM_001171933.1:c.2913+14G>A	NP_001165404.1:n.2913+14G>A
NM_001171934.1:c.2913+14G>A	NP_001165405.1:n.2913+14G>A
NM_001171935.1:c.324+14G>A	NP_001165406.1:n.324+14G>A
NM_001171936.1:c.324+14G>A	NP_001165407.1:n.324+14G>A
NM_022124.5:c.9633+14G>A	NP_071407.4:n.9633+14G>A
ENST00000224721.10:c.9648+14G>A	ENSP00000224721.8:n.9648+14G>A
ENST00000398788.4:c.2913+14G>A	ENSP00000381768.3:n.2913+14G>A
ENST00000475158.1:n.3169+14G>A
ENST00000619887.4:c.2913+14G>A	ENSP00000478374.1:n.2913+14G>A
ENST00000622827.4:c.9633+14G>A	ENSP00000483211.1:n.9633+14G>A
ENST00000642965.1:c.3566+14G>A	ENSP00000495222.1:n.3566+14G>A
ENST00000647092.1:c.3230+14G>A	ENSP00000495176.1:n.3230+14G>A
XM_006717940.2:c.9828+14G>A	XP_006718003.1:n.9828+14G>A
XM_006717942.2:c.9762+14G>A	XP_006718005.1:n.9762+14G>A
XM_011540039.1:c.9825+14G>A	XP_011538341.1:n.9825+14G>A
XM_011540040.1:c.9822+14G>A	XP_011538342.1:n.9822+14G>A
XM_011540041.1:c.9768+14G>A	XP_011538343.1:n.9768+14G>A
XM_011540042.1:c.9738+14G>A	XP_011538344.1:n.9738+14G>A
XM_011540043.1:c.9828+14G>A	XP_011538345.1:n.9828+14G>A
XM_011540044.1:c.9693+14G>A	XP_011538346.1:n.9693+14G>A
XM_011540045.1:c.9828+14G>A	XP_011538347.1:n.9828+14G>A
XM_011540046.1:c.9288+14G>A	XP_011538348.1:n.9288+14G>A
XM_011540047.1:c.8646+14G>A	XP_011538349.1:n.8646+14G>A
XM_011540052.1:c.6156+14G>A	XP_011538354.1:n.6156+14G>A