Canonical Allele Identifier: CA594705676

Gene: CDH23

Linked Data

• dbSNP Id: rs1370400845
• gnomAD v2: 10-73405429-G-GCTGCTCTGGGAAAGCC
• gnomAD v4: 10-71645672-G-GCTGCTCTGGGAAAGCC
• MyVariant Identifiers: chr10:g.73405429_73405430insCTGCTCTGGGAAAGCC (hg19) ; chr10:g.71645672_71645673insCTGCTCTGGGAAAGCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71645681_71645696dup , CM000672.2:g.71645681_71645696dup	GRCh38
NC_000010.10:g.73405438_73405453dup , CM000672.1:g.73405438_73405453dup	GRCh37
NC_000010.9:g.73075444_73075459dup	NCBI36
NG_008835.1:g.253735_253750dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.1141-150_1141-135dup MANE Select	ENSP00000224721.9:n.1141-150_1141-135dup
ENST00000398809.9:c.1141-150_1141-135dup	ENSP00000381789.5:n.1141-150_1141-135dup
ENST00000442677.4:c.1141-150_1141-135dup	ENSP00000388894.3:n.1141-150_1141-135dup
ENST00000466757.8:c.572-150_572-135dup
ENST00000643732.1:n.977-150_977-135dup
ENST00000646131.1:c.805-150_805-135dup	ENSP00000495098.1:n.805-150_805-135dup
ENST00000224721.10:c.1156-150_1156-135dup	ENSP00000224721.8:n.1156-150_1156-135dup
ENST00000299366.11:c.1141-150_1141-135dup	ENSP00000299366.8:n.1141-150_1141-135dup
ENST00000398809.8:c.1141-150_1141-135dup	ENSP00000381789.5:n.1141-150_1141-135dup
ENST00000398842.7:c.886-150_886-135dup	ENSP00000381822.4:n.886-150_886-135dup
ENST00000461841.7:c.1141-150_1141-135dup	ENSP00000473454.2:n.1141-150_1141-135dup
ENST00000466757.7:c.572-150_572-135dup
ENST00000470494.5:c.110-150_110-135dup
ENST00000616684.4:c.1141-150_1141-135dup	ENSP00000482036.2:n.1141-150_1141-135dup
ENST00000622827.4:c.1135-144_1135-129dup	ENSP00000483211.1:n.1135-144_1135-129dup
NM_001171930.1:c.1141-150_1141-135dup	NP_001165401.1:n.1141-150_1141-135dup
NM_001171931.1:c.1141-150_1141-135dup	NP_001165402.1:n.1141-150_1141-135dup
NM_022124.5:c.1141-150_1141-135dup	NP_071407.4:n.1141-150_1141-135dup
NM_052836.3:c.1141-150_1141-135dup	NP_443068.1:n.1141-150_1141-135dup
XM_006717940.2:c.1336-150_1336-135dup	XP_006718003.1:n.1336-150_1336-135dup
XM_006717942.2:c.1270-150_1270-135dup	XP_006718005.1:n.1270-150_1270-135dup
XM_011540039.1:c.1336-150_1336-135dup	XP_011538341.1:n.1336-150_1336-135dup
XM_011540040.1:c.1330-150_1330-135dup	XP_011538342.1:n.1330-150_1330-135dup
XM_011540041.1:c.1276-150_1276-135dup	XP_011538343.1:n.1276-150_1276-135dup
XM_011540042.1:c.1336-150_1336-135dup	XP_011538344.1:n.1336-150_1336-135dup
XM_011540043.1:c.1336-150_1336-135dup	XP_011538345.1:n.1336-150_1336-135dup
XM_011540044.1:c.1201-150_1201-135dup	XP_011538346.1:n.1201-150_1201-135dup
XM_011540045.1:c.1336-150_1336-135dup	XP_011538347.1:n.1336-150_1336-135dup
XM_011540046.1:c.796-150_796-135dup	XP_011538348.1:n.796-150_796-135dup
XM_011540047.1:c.154-150_154-135dup	XP_011538349.1:n.154-150_154-135dup
XM_011540048.1:c.1336-150_1336-135dup	XP_011538350.1:n.1336-150_1336-135dup
XM_011540049.1:c.1336-150_1336-135dup	XP_011538351.1:n.1336-150_1336-135dup
XM_011540050.1:c.1336-150_1336-135dup	XP_011538352.1:n.1336-150_1336-135dup
XM_011540051.1:c.1336-150_1336-135dup	XP_011538353.1:n.1336-150_1336-135dup
XM_011540053.1:c.1336-150_1336-135dup	XP_011538355.1:n.1336-150_1336-135dup
XM_011540054.1:c.1276-150_1276-135dup	XP_011538356.1:n.1276-150_1276-135dup
XR_945796.1:n.1579-150_1579-135dup
NM_001171930.2:c.1141-150_1141-135dup	NP_001165401.1:n.1141-150_1141-135dup
NM_001171931.2:c.1141-150_1141-135dup	NP_001165402.1:n.1141-150_1141-135dup
NM_022124.6:c.1141-150_1141-135dup MANE Select	NP_071407.4:n.1141-150_1141-135dup
NM_052836.4:c.1141-150_1141-135dup	NP_443068.1:n.1141-150_1141-135dup