Canonical Allele Identifier: CA1918809273

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71645916C= , CM000672.2:g.71645916C=	GRCh38
NC_000010.10:g.73405673C= , CM000672.1:g.73405673C=	GRCh37
NC_000010.9:g.73075679C=	NCBI36
NG_008835.1:g.253970C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.1226C= MANE Select	ENSP00000224721.9:p.Ala409=
ENST00000398809.9:c.1226C=	ENSP00000381789.5:p.Ala409=
ENST00000442677.4:c.1226C=	ENSP00000388894.3:p.Ala409=
ENST00000466757.8:c.657C=
ENST00000643732.1:n.1062C=
ENST00000646131.1:c.890C=	ENSP00000495098.1:p.Ala297=
ENST00000224721.10:c.1241C=	ENSP00000224721.8:p.Ala414=
ENST00000299366.11:c.1226C=	ENSP00000299366.8:p.Ala409=
ENST00000398809.8:c.1226C=	ENSP00000381789.5:p.Ala409=
ENST00000398842.7:c.971C=	ENSP00000381822.4:p.Ala324=
ENST00000442677.3:c.1C=
ENST00000461841.7:c.1226C=	ENSP00000473454.2:p.Ala409=
ENST00000466757.7:c.657C=
ENST00000470494.5:c.195C=
ENST00000616684.4:c.1226C=	ENSP00000482036.2:p.Ala409=
ENST00000622827.4:c.1226C=	ENSP00000483211.1:p.Ala409=
NM_001171930.1:c.1226C=	NP_001165401.1:p.Ala409=
NM_001171931.1:c.1226C=	NP_001165402.1:p.Ala409=
NM_022124.5:c.1226C=	NP_071407.4:p.Ala409=
NM_052836.3:c.1226C=	NP_443068.1:p.Ala409=
XM_006717940.2:c.1421C=	XP_006718003.1:p.Ala474=
XM_006717942.2:c.1355C=	XP_006718005.1:p.Ala452=
XM_011540039.1:c.1421C=	XP_011538341.1:p.Ala474=
XM_011540040.1:c.1415C=	XP_011538342.1:p.Ala472=
XM_011540041.1:c.1361C=	XP_011538343.1:p.Ala454=
XM_011540042.1:c.1421C=	XP_011538344.1:p.Ala474=
XM_011540043.1:c.1421C=	XP_011538345.1:p.Ala474=
XM_011540044.1:c.1286C=	XP_011538346.1:p.Ala429=
XM_011540045.1:c.1421C=	XP_011538347.1:p.Ala474=
XM_011540046.1:c.881C=	XP_011538348.1:p.Ala294=
XM_011540047.1:c.239C=	XP_011538349.1:p.Ala80=
XM_011540048.1:c.1421C=	XP_011538350.1:p.Ala474=
XM_011540049.1:c.1421C=	XP_011538351.1:p.Ala474=
XM_011540050.1:c.1421C=	XP_011538352.1:p.Ala474=
XM_011540051.1:c.1421C=	XP_011538353.1:p.Ala474=
XM_011540053.1:c.1421C=	XP_011538355.1:p.Ala474=
XM_011540054.1:c.1361C=	XP_011538356.1:p.Ala454=
XR_945796.1:n.1664C=
NM_001171930.2:c.1226C=	NP_001165401.1:p.Ala409=
NM_001171931.2:c.1226C=	NP_001165402.1:p.Ala409=
NM_022124.6:c.1226C= MANE Select	NP_071407.4:p.Ala409=
NM_052836.4:c.1226C=	NP_443068.1:p.Ala409=