Canonical Allele Identifier: CA377154249

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73552998G>T (hg19) ; chr10:g.71793241G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793241G>T , CM000672.2:g.71793241G>T	GRCh38
NC_000010.10:g.73552998G>T , CM000672.1:g.73552998G>T	GRCh37
NC_000010.9:g.73223004G>T	NCBI36
NG_008835.1:g.401295G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6313G>T MANE Select	ENSP00000224721.9:p.Val2105Phe
ENST00000224721.10:c.6328G>T	ENSP00000224721.8:p.Val2110Phe
ENST00000622827.4:c.6313G>T	ENSP00000483211.1:p.Val2105Phe
NM_022124.5:c.6313G>T	NP_071407.4:p.Val2105Phe
XM_006717940.2:c.6508G>T	XP_006718003.1:p.Val2170Phe
XM_006717942.2:c.6442G>T	XP_006718005.1:p.Val2148Phe
XM_011540039.1:c.6505G>T	XP_011538341.1:p.Val2169Phe
XM_011540040.1:c.6502G>T	XP_011538342.1:p.Val2168Phe
XM_011540041.1:c.6448G>T	XP_011538343.1:p.Val2150Phe
XM_011540042.1:c.6508G>T	XP_011538344.1:p.Val2170Phe
XM_011540043.1:c.6508G>T	XP_011538345.1:p.Val2170Phe
XM_011540044.1:c.6373G>T	XP_011538346.1:p.Val2125Phe
XM_011540045.1:c.6508G>T	XP_011538347.1:p.Val2170Phe
XM_011540046.1:c.5968G>T	XP_011538348.1:p.Val1990Phe
XM_011540047.1:c.5326G>T	XP_011538349.1:p.Val1776Phe
XM_011540048.1:c.6508G>T	XP_011538350.1:p.Val2170Phe
XM_011540049.1:c.6508G>T	XP_011538351.1:p.Val2170Phe
XM_011540050.1:c.6508G>T	XP_011538352.1:p.Val2170Phe
XM_011540051.1:c.6508G>T	XP_011538353.1:p.Val2170Phe
XM_011540052.1:c.2836G>T	XP_011538354.1:p.Val946Phe
XR_945796.1:n.6751G>T
NM_022124.6:c.6313G>T MANE Select	NP_071407.4:p.Val2105Phe