Canonical Allele Identifier: CA1918809296

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71645960G= , CM000672.2:g.71645960G=	GRCh38
NC_000010.10:g.73405717G= , CM000672.1:g.73405717G=	GRCh37
NC_000010.9:g.73075723G=	NCBI36
NG_008835.1:g.254014G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.1270G= MANE Select	ENSP00000224721.9:p.Val424=
ENST00000398809.9:c.1270G=	ENSP00000381789.5:p.Val424=
ENST00000442677.4:c.1270G=	ENSP00000388894.3:p.Val424=
ENST00000466757.8:c.701G=
ENST00000643732.1:n.1106G=
ENST00000646131.1:c.934G=	ENSP00000495098.1:p.Val312=
ENST00000224721.10:c.1285G=	ENSP00000224721.8:p.Val429=
ENST00000299366.11:c.1270G=	ENSP00000299366.8:p.Val424=
ENST00000398809.8:c.1270G=	ENSP00000381789.5:p.Val424=
ENST00000398842.7:c.1015G=	ENSP00000381822.4:p.Val339=
ENST00000442677.3:c.45G=
ENST00000461841.7:c.1270G=	ENSP00000473454.2:p.Val424=
ENST00000466757.7:c.701G=
ENST00000470494.5:c.239G=
ENST00000616684.4:c.1270G=	ENSP00000482036.2:p.Val424=
ENST00000622827.4:c.1270G=	ENSP00000483211.1:p.Val424=
NM_001171930.1:c.1270G=	NP_001165401.1:p.Val424=
NM_001171931.1:c.1270G=	NP_001165402.1:p.Val424=
NM_022124.5:c.1270G=	NP_071407.4:p.Val424=
NM_052836.3:c.1270G=	NP_443068.1:p.Val424=
XM_006717940.2:c.1465G=	XP_006718003.1:p.Val489=
XM_006717942.2:c.1399G=	XP_006718005.1:p.Val467=
XM_011540039.1:c.1465G=	XP_011538341.1:p.Val489=
XM_011540040.1:c.1459G=	XP_011538342.1:p.Val487=
XM_011540041.1:c.1405G=	XP_011538343.1:p.Val469=
XM_011540042.1:c.1465G=	XP_011538344.1:p.Val489=
XM_011540043.1:c.1465G=	XP_011538345.1:p.Val489=
XM_011540044.1:c.1330G=	XP_011538346.1:p.Val444=
XM_011540045.1:c.1465G=	XP_011538347.1:p.Val489=
XM_011540046.1:c.925G=	XP_011538348.1:p.Val309=
XM_011540047.1:c.283G=	XP_011538349.1:p.Val95=
XM_011540048.1:c.1465G=	XP_011538350.1:p.Val489=
XM_011540049.1:c.1465G=	XP_011538351.1:p.Val489=
XM_011540050.1:c.1465G=	XP_011538352.1:p.Val489=
XM_011540051.1:c.1465G=	XP_011538353.1:p.Val489=
XM_011540053.1:c.1465G=	XP_011538355.1:p.Val489=
XM_011540054.1:c.1405G=	XP_011538356.1:p.Val469=
XR_945796.1:n.1708G=
NM_001171930.2:c.1270G=	NP_001165401.1:p.Val424=
NM_001171931.2:c.1270G=	NP_001165402.1:p.Val424=
NM_022124.6:c.1270G= MANE Select	NP_071407.4:p.Val424=
NM_052836.4:c.1270G=	NP_443068.1:p.Val424=