Canonical Allele Identifier: CA470062372

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73468883G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71709126G>T , CM000672.2:g.71709126G>T	GRCh38
NC_000010.10:g.73468883G>T , CM000672.1:g.73468883G>T	GRCh37
NC_000010.9:g.73138889G>T	NCBI36
NG_008835.1:g.317180G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.3135G>T MANE Select	ENSP00000224721.9:p.Val1045=
ENST00000398809.9:c.3135G>T	ENSP00000381789.5:p.Val1045=
ENST00000442677.4:c.3135G>T	ENSP00000388894.3:p.Val1045=
ENST00000466757.8:c.2566G>T
ENST00000224721.10:c.3150G>T	ENSP00000224721.8:p.Val1050=
ENST00000398809.8:c.3135G>T	ENSP00000381789.5:p.Val1045=
ENST00000442677.3:c.1910G>T
ENST00000466757.7:c.2566G>T
ENST00000616684.4:c.3135G>T	ENSP00000482036.2:p.Val1045=
ENST00000622827.4:c.3135G>T	ENSP00000483211.1:p.Val1045=
NM_001171930.1:c.3135G>T	NP_001165401.1:p.Val1045=
NM_022124.5:c.3135G>T	NP_071407.4:p.Val1045=
XM_006717940.2:c.3330G>T	XP_006718003.1:p.Val1110=
XM_006717942.2:c.3264G>T	XP_006718005.1:p.Val1088=
XM_011540039.1:c.3330G>T	XP_011538341.1:p.Val1110=
XM_011540040.1:c.3324G>T	XP_011538342.1:p.Val1108=
XM_011540041.1:c.3270G>T	XP_011538343.1:p.Val1090=
XM_011540042.1:c.3330G>T	XP_011538344.1:p.Val1110=
XM_011540043.1:c.3330G>T	XP_011538345.1:p.Val1110=
XM_011540044.1:c.3195G>T	XP_011538346.1:p.Val1065=
XM_011540045.1:c.3330G>T	XP_011538347.1:p.Val1110=
XM_011540046.1:c.2790G>T	XP_011538348.1:p.Val930=
XM_011540047.1:c.2148G>T	XP_011538349.1:p.Val716=
XM_011540048.1:c.3330G>T	XP_011538350.1:p.Val1110=
XM_011540049.1:c.3330G>T	XP_011538351.1:p.Val1110=
XM_011540050.1:c.3330G>T	XP_011538352.1:p.Val1110=
XM_011540051.1:c.3330G>T	XP_011538353.1:p.Val1110=
XM_011540053.1:c.3330G>T	XP_011538355.1:p.Val1110=
XR_945796.1:n.3573G>T
NM_001171930.2:c.3135G>T	NP_001165401.1:p.Val1045=
NM_022124.6:c.3135G>T MANE Select	NP_071407.4:p.Val1045=