Canonical Allele Identifier: CA2609590732

Gene: CDH23

Linked Data

• gnomAD v4: 10-71815647-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71815647A>T , CM000672.2:g.71815647A>T	GRCh38
NC_000010.10:g.73575404A>T , CM000672.1:g.73575404A>T	GRCh37
NC_000010.9:g.73245410A>T	NCBI36
NG_008835.1:g.423701A>T
NG_009301.1:g.40679T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.*369A>T MANE Select	ENSP00000224721.9:n.*369A>T
ENST00000642965.1:c.4367A>T	ENSP00000495222.1:n.4367A>T
ENST00000647092.1:c.3926A>T	ENSP00000495176.1:n.3926A>T
ENST00000224721.10:c.*369A>T	ENSP00000224721.8:n.*369A>T
ENST00000398788.4:c.*369A>T	ENSP00000381768.3:n.*369A>T
ENST00000475158.1:n.3865A>T
ENST00000619887.4:c.*369A>T	ENSP00000478374.1:n.*369A>T
ENST00000622827.4:c.*369A>T	ENSP00000483211.1:n.*369A>T
NM_001171933.1:c.*369A>T	NP_001165404.1:n.*369A>T
NM_001171934.1:c.*369A>T	NP_001165405.1:n.*369A>T
NM_001171935.1:c.*369A>T	NP_001165406.1:n.*369A>T
NM_001171936.1:c.*369A>T	NP_001165407.1:n.*369A>T
NM_022124.5:c.*369A>T	NP_071407.4:n.*369A>T
XM_006717940.2:c.*369A>T	XP_006718003.1:n.*369A>T
XM_006717942.2:c.*369A>T	XP_006718005.1:n.*369A>T
XM_011540039.1:c.*369A>T	XP_011538341.1:n.*369A>T
XM_011540040.1:c.*369A>T	XP_011538342.1:n.*369A>T
XM_011540041.1:c.*369A>T	XP_011538343.1:n.*369A>T
XM_011540042.1:c.*369A>T	XP_011538344.1:n.*369A>T
XM_011540043.1:c.*369A>T	XP_011538345.1:n.*369A>T
XM_011540044.1:c.*369A>T	XP_011538346.1:n.*369A>T
XM_011540046.1:c.*369A>T	XP_011538348.1:n.*369A>T
XM_011540047.1:c.*369A>T	XP_011538349.1:n.*369A>T
XM_011540052.1:c.*369A>T	XP_011538354.1:n.*369A>T
NM_022124.6:c.*369A>T MANE Select	NP_071407.4:n.*369A>T