Canonical Allele Identifier: CA377158089

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73558249C>A (hg19) ; chr10:g.71798492C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798492C>A , CM000672.2:g.71798492C>A	GRCh38
NC_000010.10:g.73558249C>A , CM000672.1:g.73558249C>A	GRCh37
NC_000010.9:g.73228255C>A	NCBI36
NG_008835.1:g.406546C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6968C>A MANE Select	ENSP00000224721.9:p.Pro2323His
ENST00000642965.1:c.901C>A	ENSP00000495222.1:n.901C>A
ENST00000647092.1:c.565C>A	ENSP00000495176.1:n.565C>A
ENST00000224721.10:c.6983C>A	ENSP00000224721.8:p.Pro2328His
ENST00000398788.4:c.248C>A	ENSP00000381768.3:p.Pro83His
ENST00000475158.1:n.504C>A
ENST00000619887.4:c.248C>A	ENSP00000478374.1:p.Pro83His
ENST00000622827.4:c.6968C>A	ENSP00000483211.1:p.Pro2323His
NM_001171933.1:c.248C>A	NP_001165404.1:p.Pro83His
NM_001171934.1:c.248C>A	NP_001165405.1:p.Pro83His
NM_022124.5:c.6968C>A	NP_071407.4:p.Pro2323His
XM_006717940.2:c.7163C>A	XP_006718003.1:p.Pro2388His
XM_006717942.2:c.7097C>A	XP_006718005.1:p.Pro2366His
XM_011540039.1:c.7160C>A	XP_011538341.1:p.Pro2387His
XM_011540040.1:c.7157C>A	XP_011538342.1:p.Pro2386His
XM_011540041.1:c.7103C>A	XP_011538343.1:p.Pro2368His
XM_011540042.1:c.7073C>A	XP_011538344.1:p.Pro2358His
XM_011540043.1:c.7163C>A	XP_011538345.1:p.Pro2388His
XM_011540044.1:c.7028C>A	XP_011538346.1:p.Pro2343His
XM_011540045.1:c.7163C>A	XP_011538347.1:p.Pro2388His
XM_011540046.1:c.6623C>A	XP_011538348.1:p.Pro2208His
XM_011540047.1:c.5981C>A	XP_011538349.1:p.Pro1994His
XM_011540052.1:c.3491C>A	XP_011538354.1:p.Pro1164His
NM_022124.6:c.6968C>A MANE Select	NP_071407.4:p.Pro2323His