Canonical Allele Identifier: CA377159298

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73559295T>A (hg19) ; chr10:g.71799538T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71799538T>A , CM000672.2:g.71799538T>A	GRCh38
NC_000010.10:g.73559295T>A , CM000672.1:g.73559295T>A	GRCh37
NC_000010.9:g.73229301T>A	NCBI36
NG_008835.1:g.407592T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7271T>A MANE Select	ENSP00000224721.9:p.Val2424Asp
ENST00000642965.1:c.1204T>A	ENSP00000495222.1:n.1204T>A
ENST00000647092.1:c.868T>A	ENSP00000495176.1:n.868T>A
ENST00000224721.10:c.7286T>A	ENSP00000224721.8:p.Val2429Asp
ENST00000398788.4:c.551T>A	ENSP00000381768.3:p.Val184Asp
ENST00000475158.1:n.807T>A
ENST00000619887.4:c.551T>A	ENSP00000478374.1:p.Val184Asp
ENST00000622827.4:c.7271T>A	ENSP00000483211.1:p.Val2424Asp
NM_001171933.1:c.551T>A	NP_001165404.1:p.Val184Asp
NM_001171934.1:c.551T>A	NP_001165405.1:p.Val184Asp
NM_022124.5:c.7271T>A	NP_071407.4:p.Val2424Asp
XM_006717940.2:c.7466T>A	XP_006718003.1:p.Val2489Asp
XM_006717942.2:c.7400T>A	XP_006718005.1:p.Val2467Asp
XM_011540039.1:c.7463T>A	XP_011538341.1:p.Val2488Asp
XM_011540040.1:c.7460T>A	XP_011538342.1:p.Val2487Asp
XM_011540041.1:c.7406T>A	XP_011538343.1:p.Val2469Asp
XM_011540042.1:c.7376T>A	XP_011538344.1:p.Val2459Asp
XM_011540043.1:c.7466T>A	XP_011538345.1:p.Val2489Asp
XM_011540044.1:c.7331T>A	XP_011538346.1:p.Val2444Asp
XM_011540045.1:c.7466T>A	XP_011538347.1:p.Val2489Asp
XM_011540046.1:c.6926T>A	XP_011538348.1:p.Val2309Asp
XM_011540047.1:c.6284T>A	XP_011538349.1:p.Val2095Asp
XM_011540052.1:c.3794T>A	XP_011538354.1:p.Val1265Asp
NM_022124.6:c.7271T>A MANE Select	NP_071407.4:p.Val2424Asp