Canonical Allele Identifier: CA1918769569

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71570758C= , CM000672.2:g.71570758C=	GRCh38
NC_000010.10:g.73330515C= , CM000672.1:g.73330515C=	GRCh37
NC_000010.9:g.73000521C=	NCBI36
NG_008835.1:g.178812C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.625-32C= MANE Select	ENSP00000224721.9:n.625-32C=
ENST00000398809.9:c.625-32C=	ENSP00000381789.5:n.625-32C=
ENST00000442677.4:c.625-32C=	ENSP00000388894.3:n.625-32C=
ENST00000643732.1:n.401-32C=
ENST00000646131.1:c.289-32C=	ENSP00000495098.1:n.289-32C=
ENST00000224721.10:c.640-32C=	ENSP00000224721.8:n.640-32C=
ENST00000299366.11:c.625-32C=	ENSP00000299366.8:n.625-32C=
ENST00000398809.8:c.625-32C=	ENSP00000381789.5:n.625-32C=
ENST00000398842.7:c.444-70C=	ENSP00000381822.4:n.444-70C=
ENST00000461841.7:c.625-32C=	ENSP00000473454.2:n.625-32C=
ENST00000616684.4:c.625-32C=	ENSP00000482036.2:n.625-32C=
ENST00000622827.4:c.625-32C=	ENSP00000483211.1:n.625-32C=
NM_001171930.1:c.625-32C=	NP_001165401.1:n.625-32C=
NM_001171931.1:c.625-32C=	NP_001165402.1:n.625-32C=
NM_001171932.1:c.625-32C=	NP_001165403.1:n.625-32C=
NM_022124.5:c.625-32C=	NP_071407.4:n.625-32C=
NM_052836.3:c.625-32C=	NP_443068.1:n.625-32C=
XM_006717940.2:c.760-32C=	XP_006718003.1:n.760-32C=
XM_006717942.2:c.760-32C=	XP_006718005.1:n.760-32C=
XM_011540039.1:c.760-32C=	XP_011538341.1:n.760-32C=
XM_011540040.1:c.760-32C=	XP_011538342.1:n.760-32C=
XM_011540041.1:c.760-32C=	XP_011538343.1:n.760-32C=
XM_011540042.1:c.760-32C=	XP_011538344.1:n.760-32C=
XM_011540043.1:c.760-32C=	XP_011538345.1:n.760-32C=
XM_011540044.1:c.625-32C=	XP_011538346.1:n.625-32C=
XM_011540045.1:c.760-32C=	XP_011538347.1:n.760-32C=
XM_011540046.1:c.220-32C=	XP_011538348.1:n.220-32C=
XM_011540048.1:c.760-32C=	XP_011538350.1:n.760-32C=
XM_011540049.1:c.760-32C=	XP_011538351.1:n.760-32C=
XM_011540050.1:c.760-32C=	XP_011538352.1:n.760-32C=
XM_011540051.1:c.760-32C=	XP_011538353.1:n.760-32C=
XM_011540053.1:c.760-32C=	XP_011538355.1:n.760-32C=
XM_011540054.1:c.760-32C=	XP_011538356.1:n.760-32C=
XR_246128.2:n.162-5624G=
XR_945796.1:n.1003-32C=
NM_001171930.2:c.625-32C=	NP_001165401.1:n.625-32C=
NM_001171931.2:c.625-32C=	NP_001165402.1:n.625-32C=
NM_022124.6:c.625-32C= MANE Select	NP_071407.4:n.625-32C=
NM_052836.4:c.625-32C=	NP_443068.1:n.625-32C=
NM_001171932.2:c.625-32C=	NP_001165403.1:n.625-32C=