Canonical Allele Identifier: CA470058017

Gene: CDH23

Linked Data

• gnomAD v4: 10-71645950-C-T
• MyVariant Identifiers: chr10:g.73405707C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71645950C>T , CM000672.2:g.71645950C>T	GRCh38
NC_000010.10:g.73405707C>T , CM000672.1:g.73405707C>T	GRCh37
NC_000010.9:g.73075713C>T	NCBI36
NG_008835.1:g.254004C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.1260C>T MANE Select	ENSP00000224721.9:p.Asp420=
ENST00000398809.9:c.1260C>T	ENSP00000381789.5:p.Asp420=
ENST00000442677.4:c.1260C>T	ENSP00000388894.3:p.Asp420=
ENST00000466757.8:c.691C>T
ENST00000643732.1:n.1096C>T
ENST00000646131.1:c.924C>T	ENSP00000495098.1:p.Asp308=
ENST00000224721.10:c.1275C>T	ENSP00000224721.8:p.Asp425=
ENST00000299366.11:c.1260C>T	ENSP00000299366.8:p.Asp420=
ENST00000398809.8:c.1260C>T	ENSP00000381789.5:p.Asp420=
ENST00000398842.7:c.1005C>T	ENSP00000381822.4:p.Asp335=
ENST00000442677.3:c.35C>T
ENST00000461841.7:c.1260C>T	ENSP00000473454.2:p.Asp420=
ENST00000466757.7:c.691C>T
ENST00000470494.5:c.229C>T
ENST00000616684.4:c.1260C>T	ENSP00000482036.2:p.Asp420=
ENST00000622827.4:c.1260C>T	ENSP00000483211.1:p.Asp420=
NM_001171930.1:c.1260C>T	NP_001165401.1:p.Asp420=
NM_001171931.1:c.1260C>T	NP_001165402.1:p.Asp420=
NM_022124.5:c.1260C>T	NP_071407.4:p.Asp420=
NM_052836.3:c.1260C>T	NP_443068.1:p.Asp420=
XM_006717940.2:c.1455C>T	XP_006718003.1:p.Asp485=
XM_006717942.2:c.1389C>T	XP_006718005.1:p.Asp463=
XM_011540039.1:c.1455C>T	XP_011538341.1:p.Asp485=
XM_011540040.1:c.1449C>T	XP_011538342.1:p.Asp483=
XM_011540041.1:c.1395C>T	XP_011538343.1:p.Asp465=
XM_011540042.1:c.1455C>T	XP_011538344.1:p.Asp485=
XM_011540043.1:c.1455C>T	XP_011538345.1:p.Asp485=
XM_011540044.1:c.1320C>T	XP_011538346.1:p.Asp440=
XM_011540045.1:c.1455C>T	XP_011538347.1:p.Asp485=
XM_011540046.1:c.915C>T	XP_011538348.1:p.Asp305=
XM_011540047.1:c.273C>T	XP_011538349.1:p.Asp91=
XM_011540048.1:c.1455C>T	XP_011538350.1:p.Asp485=
XM_011540049.1:c.1455C>T	XP_011538351.1:p.Asp485=
XM_011540050.1:c.1455C>T	XP_011538352.1:p.Asp485=
XM_011540051.1:c.1455C>T	XP_011538353.1:p.Asp485=
XM_011540053.1:c.1455C>T	XP_011538355.1:p.Asp485=
XM_011540054.1:c.1395C>T	XP_011538356.1:p.Asp465=
XR_945796.1:n.1698C>T
NM_001171930.2:c.1260C>T	NP_001165401.1:p.Asp420=
NM_001171931.2:c.1260C>T	NP_001165402.1:p.Asp420=
NM_022124.6:c.1260C>T MANE Select	NP_071407.4:p.Asp420=
NM_052836.4:c.1260C>T	NP_443068.1:p.Asp420=