Canonical Allele Identifier: CA137651

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71815116C>T , CM000672.2:g.71815116C>T	GRCh38
NC_000010.10:g.73574873C>T , CM000672.1:g.73574873C>T	GRCh37
NC_000010.9:g.73244879C>T	NCBI36
NG_008835.1:g.423170C>T
NG_009301.1:g.41210G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_022124.6:c.9903C>T MANE Select	NP_071407.4:p.Pro3301=
ENST00000224721.12:c.9903C>T MANE Select	ENSP00000224721.9:p.Pro3301=
NM_001171933.1:c.3183C>T	NP_001165404.1:p.Pro1061=
NM_001171934.1:c.3078C>T	NP_001165405.1:p.Pro1026=
NM_001171935.1:c.594C>T	NP_001165406.1:p.Pro198=
NM_001171936.1:c.489C>T	NP_001165407.1:p.Pro163=
NM_022124.5:c.9903C>T	NP_071407.4:p.Pro3301=
ENST00000224721.10:c.9918C>T	ENSP00000224721.8:p.Pro3306=
ENST00000398788.4:c.3183C>T	ENSP00000381768.3:p.Pro1061=
ENST00000475158.1:n.3334C>T
ENST00000619887.4:c.3078C>T	ENSP00000478374.1:p.Pro1026=
ENST00000622827.4:c.9903C>T	ENSP00000483211.1:p.Pro3301=
ENST00000642965.1:c.3836C>T	ENSP00000495222.1:n.3836C>T
ENST00000647092.1:c.3395C>T	ENSP00000495176.1:n.3395C>T
XM_006717940.2:c.10098C>T	XP_006718003.1:p.Pro3366=
XM_006717942.2:c.10032C>T	XP_006718005.1:p.Pro3344=
XM_011540039.1:c.10095C>T	XP_011538341.1:p.Pro3365=
XM_011540040.1:c.10092C>T	XP_011538342.1:p.Pro3364=
XM_011540041.1:c.10038C>T	XP_011538343.1:p.Pro3346=
XM_011540042.1:c.10008C>T	XP_011538344.1:p.Pro3336=
XM_011540043.1:c.9993C>T	XP_011538345.1:p.Pro3331=
XM_011540044.1:c.9963C>T	XP_011538346.1:p.Pro3321=
XM_011540046.1:c.9558C>T	XP_011538348.1:p.Pro3186=
XM_011540047.1:c.8916C>T	XP_011538349.1:p.Pro2972=
XM_011540052.1:c.6426C>T	XP_011538354.1:p.Pro2142=