Canonical Allele Identifier: CA137419

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71738491C>T , CM000672.2:g.71738491C>T	GRCh38
NC_000010.10:g.73498248C>T , CM000672.1:g.73498248C>T	GRCh37
NC_000010.9:g.73168254C>T	NCBI36
NG_008835.1:g.346545C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4210-7C>T MANE Select	ENSP00000224721.9:n.4210-7C>T
ENST00000224721.10:c.4225-7C>T	ENSP00000224721.8:n.4225-7C>T
ENST00000398792.3:n.899-7C>T
ENST00000622827.4:c.4207-4C>T	ENSP00000483211.1:n.4207-4C>T
NM_022124.5:c.4210-7C>T	NP_071407.4:n.4210-7C>T
XM_006717940.2:c.4405-7C>T	XP_006718003.1:n.4405-7C>T
XM_006717942.2:c.4339-7C>T	XP_006718005.1:n.4339-7C>T
XM_011540039.1:c.4402-7C>T	XP_011538341.1:n.4402-7C>T
XM_011540040.1:c.4399-7C>T	XP_011538342.1:n.4399-7C>T
XM_011540041.1:c.4345-7C>T	XP_011538343.1:n.4345-7C>T
XM_011540042.1:c.4405-7C>T	XP_011538344.1:n.4405-7C>T
XM_011540043.1:c.4405-7C>T	XP_011538345.1:n.4405-7C>T
XM_011540044.1:c.4270-7C>T	XP_011538346.1:n.4270-7C>T
XM_011540045.1:c.4405-7C>T	XP_011538347.1:n.4405-7C>T
XM_011540046.1:c.3865-7C>T	XP_011538348.1:n.3865-7C>T
XM_011540047.1:c.3223-7C>T	XP_011538349.1:n.3223-7C>T
XM_011540048.1:c.4405-7C>T	XP_011538350.1:n.4405-7C>T
XM_011540049.1:c.4405-7C>T	XP_011538351.1:n.4405-7C>T
XM_011540050.1:c.4405-7C>T	XP_011538352.1:n.4405-7C>T
XM_011540051.1:c.4405-7C>T	XP_011538353.1:n.4405-7C>T
XM_011540052.1:c.733-7C>T	XP_011538354.1:n.733-7C>T
XM_011540053.1:c.4405-7C>T	XP_011538355.1:n.4405-7C>T
XR_945796.1:n.4648-7C>T
NM_022124.6:c.4210-7C>T MANE Select	NP_071407.4:n.4210-7C>T