Canonical Allele Identifier: CA1918880473

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71803097C= , CM000672.2:g.71803097C=	GRCh38
NC_000010.10:g.73562854C= , CM000672.1:g.73562854C=	GRCh37
NC_000010.9:g.73232860C=	NCBI36
NG_008835.1:g.411151C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7660+22C= MANE Select	ENSP00000224721.9:n.7660+22C=
ENST00000642965.1:c.1593+22C=	ENSP00000495222.1:n.1593+22C=
ENST00000647092.1:c.1257+22C=	ENSP00000495176.1:n.1257+22C=
ENST00000224721.10:c.7675+22C=	ENSP00000224721.8:n.7675+22C=
ENST00000398788.4:c.940+22C=	ENSP00000381768.3:n.940+22C=
ENST00000475158.1:n.1196+22C=
ENST00000619887.4:c.940+22C=	ENSP00000478374.1:n.940+22C=
ENST00000622827.4:c.7660+22C=	ENSP00000483211.1:n.7660+22C=
NM_001171933.1:c.940+22C=	NP_001165404.1:n.940+22C=
NM_001171934.1:c.940+22C=	NP_001165405.1:n.940+22C=
NM_022124.5:c.7660+22C=	NP_071407.4:n.7660+22C=
XM_006717940.2:c.7855+22C=	XP_006718003.1:n.7855+22C=
XM_006717942.2:c.7789+22C=	XP_006718005.1:n.7789+22C=
XM_011540039.1:c.7852+22C=	XP_011538341.1:n.7852+22C=
XM_011540040.1:c.7849+22C=	XP_011538342.1:n.7849+22C=
XM_011540041.1:c.7795+22C=	XP_011538343.1:n.7795+22C=
XM_011540042.1:c.7765+22C=	XP_011538344.1:n.7765+22C=
XM_011540043.1:c.7855+22C=	XP_011538345.1:n.7855+22C=
XM_011540044.1:c.7720+22C=	XP_011538346.1:n.7720+22C=
XM_011540045.1:c.7855+22C=	XP_011538347.1:n.7855+22C=
XM_011540046.1:c.7315+22C=	XP_011538348.1:n.7315+22C=
XM_011540047.1:c.6673+22C=	XP_011538349.1:n.6673+22C=
XM_011540052.1:c.4183+22C=	XP_011538354.1:n.4183+22C=
NM_022124.6:c.7660+22C= MANE Select	NP_071407.4:n.7660+22C=