Canonical Allele Identifier: CA16605679

Gene: CDH23

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798579G>A , CM000672.2:g.71798579G>A	GRCh38
NC_000010.10:g.73558336G>A , CM000672.1:g.73558336G>A	GRCh37
NC_000010.9:g.73228342G>A	NCBI36
NG_008835.1:g.406633G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7054+1G>A MANE Select	ENSP00000224721.9:n.7054+1G>A
ENST00000642965.1:c.987+1G>A	ENSP00000495222.1:n.987+1G>A
ENST00000647092.1:c.651+1G>A	ENSP00000495176.1:n.651+1G>A
ENST00000224721.10:c.7069+1G>A	ENSP00000224721.8:n.7069+1G>A
ENST00000398788.4:c.334+1G>A	ENSP00000381768.3:n.334+1G>A
ENST00000475158.1:n.590+1G>A
ENST00000619887.4:c.334+1G>A	ENSP00000478374.1:n.334+1G>A
ENST00000622827.4:c.7054+1G>A	ENSP00000483211.1:n.7054+1G>A
NM_001171933.1:c.334+1G>A	NP_001165404.1:n.334+1G>A
NM_001171934.1:c.334+1G>A	NP_001165405.1:n.334+1G>A
NM_022124.5:c.7054+1G>A	NP_071407.4:n.7054+1G>A
XM_006717940.2:c.7249+1G>A	XP_006718003.1:n.7249+1G>A
XM_006717942.2:c.7183+1G>A	XP_006718005.1:n.7183+1G>A
XM_011540039.1:c.7246+1G>A	XP_011538341.1:n.7246+1G>A
XM_011540040.1:c.7243+1G>A	XP_011538342.1:n.7243+1G>A
XM_011540041.1:c.7189+1G>A	XP_011538343.1:n.7189+1G>A
XM_011540042.1:c.7159+1G>A	XP_011538344.1:n.7159+1G>A
XM_011540043.1:c.7249+1G>A	XP_011538345.1:n.7249+1G>A
XM_011540044.1:c.7114+1G>A	XP_011538346.1:n.7114+1G>A
XM_011540045.1:c.7249+1G>A	XP_011538347.1:n.7249+1G>A
XM_011540046.1:c.6709+1G>A	XP_011538348.1:n.6709+1G>A
XM_011540047.1:c.6067+1G>A	XP_011538349.1:n.6067+1G>A
XM_011540052.1:c.3577+1G>A	XP_011538354.1:n.3577+1G>A
NM_022124.6:c.7054+1G>A MANE Select	NP_071407.4:n.7054+1G>A