Canonical Allele Identifier: CA2788486783

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798347A>T , CM000672.2:g.71798347A>T	GRCh38
NC_000010.10:g.73558104A>T , CM000672.1:g.73558104A>T	GRCh37
NC_000010.9:g.73228110A>T	NCBI36
NG_008835.1:g.406401A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6830-7A>T MANE Select	ENSP00000224721.9:n.6830-7A>T
ENST00000642965.1:c.763-7A>T	ENSP00000495222.1:n.763-7A>T
ENST00000647092.1:c.427-7A>T	ENSP00000495176.1:n.427-7A>T
ENST00000224721.10:c.6845-7A>T	ENSP00000224721.8:n.6845-7A>T
ENST00000398788.4:c.110-7A>T	ENSP00000381768.3:n.110-7A>T
ENST00000475158.1:n.366-7A>T
ENST00000619887.4:c.110-7A>T	ENSP00000478374.1:n.110-7A>T
ENST00000622827.4:c.6830-7A>T	ENSP00000483211.1:n.6830-7A>T
NM_001171933.1:c.110-7A>T	NP_001165404.1:n.110-7A>T
NM_001171934.1:c.110-7A>T	NP_001165405.1:n.110-7A>T
NM_022124.5:c.6830-7A>T	NP_071407.4:n.6830-7A>T
XM_006717940.2:c.7025-7A>T	XP_006718003.1:n.7025-7A>T
XM_006717942.2:c.6959-7A>T	XP_006718005.1:n.6959-7A>T
XM_011540039.1:c.7022-7A>T	XP_011538341.1:n.7022-7A>T
XM_011540040.1:c.7019-7A>T	XP_011538342.1:n.7019-7A>T
XM_011540041.1:c.6965-7A>T	XP_011538343.1:n.6965-7A>T
XM_011540042.1:c.6935-7A>T	XP_011538344.1:n.6935-7A>T
XM_011540043.1:c.7025-7A>T	XP_011538345.1:n.7025-7A>T
XM_011540044.1:c.6890-7A>T	XP_011538346.1:n.6890-7A>T
XM_011540045.1:c.7025-7A>T	XP_011538347.1:n.7025-7A>T
XM_011540046.1:c.6485-7A>T	XP_011538348.1:n.6485-7A>T
XM_011540047.1:c.5843-7A>T	XP_011538349.1:n.5843-7A>T
XM_011540052.1:c.3353-7A>T	XP_011538354.1:n.3353-7A>T
NM_022124.6:c.6830-7A>T MANE Select	NP_071407.4:n.6830-7A>T