Canonical Allele Identifier: CA5544503

Gene: CDH23

Linked Data

• ClinVar Variation Id: 1254478
• ClinVar RCV Id: RCV001832840 ; RCV001665403
• dbSNP Id: rs536438868
• ExAC: 10:73468927 G / A
• gnomAD v2: 10-73468927-G-A
• gnomAD v3: 10-71709170-G-A
• gnomAD v4: 10-71709170-G-A
• MyVariant Identifiers: chr10:g.73468927G>A (hg19) ; chr10:g.71709170G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71709170G>A , CM000672.2:g.71709170G>A	GRCh38
NC_000010.10:g.73468927G>A , CM000672.1:g.73468927G>A	GRCh37
NC_000010.9:g.73138933G>A	NCBI36
NG_008835.1:g.317224G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.3179G>A MANE Select	ENSP00000224721.9:p.Arg1060Gln
ENST00000398809.9:c.3179G>A	ENSP00000381789.5:p.Arg1060Gln
ENST00000442677.4:c.3179G>A	ENSP00000388894.3:p.Arg1060Gln
ENST00000466757.8:c.2610G>A
ENST00000224721.10:c.3194G>A	ENSP00000224721.8:p.Arg1065Gln
ENST00000398809.8:c.3179G>A	ENSP00000381789.5:p.Arg1060Gln
ENST00000442677.3:c.1954G>A
ENST00000466757.7:c.2610G>A
ENST00000616684.4:c.3179G>A	ENSP00000482036.2:p.Arg1060Gln
ENST00000622827.4:c.3179G>A	ENSP00000483211.1:p.Arg1060Gln
NM_001171930.1:c.3179G>A	NP_001165401.1:p.Arg1060Gln
NM_022124.5:c.3179G>A	NP_071407.4:p.Arg1060Gln
XM_006717940.2:c.3374G>A	XP_006718003.1:p.Arg1125Gln
XM_006717942.2:c.3308G>A	XP_006718005.1:p.Arg1103Gln
XM_011540039.1:c.3374G>A	XP_011538341.1:p.Arg1125Gln
XM_011540040.1:c.3368G>A	XP_011538342.1:p.Arg1123Gln
XM_011540041.1:c.3314G>A	XP_011538343.1:p.Arg1105Gln
XM_011540042.1:c.3374G>A	XP_011538344.1:p.Arg1125Gln
XM_011540043.1:c.3374G>A	XP_011538345.1:p.Arg1125Gln
XM_011540044.1:c.3239G>A	XP_011538346.1:p.Arg1080Gln
XM_011540045.1:c.3374G>A	XP_011538347.1:p.Arg1125Gln
XM_011540046.1:c.2834G>A	XP_011538348.1:p.Arg945Gln
XM_011540047.1:c.2192G>A	XP_011538349.1:p.Arg731Gln
XM_011540048.1:c.3374G>A	XP_011538350.1:p.Arg1125Gln
XM_011540049.1:c.3374G>A	XP_011538351.1:p.Arg1125Gln
XM_011540050.1:c.3374G>A	XP_011538352.1:p.Arg1125Gln
XM_011540051.1:c.3374G>A	XP_011538353.1:p.Arg1125Gln
XM_011540053.1:c.3374G>A	XP_011538355.1:p.Arg1125Gln
XR_945796.1:n.3617G>A
NM_001171930.2:c.3179G>A	NP_001165401.1:p.Arg1060Gln
NM_022124.6:c.3179G>A MANE Select	NP_071407.4:p.Arg1060Gln