Canonical Allele Identifier: CA175521

Gene: CDH23

Linked Data

• ClinVar Variation Id: 162944
• ClinVar RCV Id: RCV000150320
• dbSNP Id: rs374011250
• ExAC: 10:73562845 C / T
• gnomAD v2: 10-73562845-C-T
• gnomAD v3: 10-71803088-C-T
• gnomAD v4: 10-71803088-C-T
• MyVariant Identifiers: chr10:g.73562845C>T (hg19) ; chr10:g.71803088C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71803088C>T , CM000672.2:g.71803088C>T	GRCh38
NC_000010.10:g.73562845C>T , CM000672.1:g.73562845C>T	GRCh37
NC_000010.9:g.73232851C>T	NCBI36
NG_008835.1:g.411142C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7660+13C>T MANE Select	ENSP00000224721.9:n.7660+13C>T
ENST00000642965.1:c.1593+13C>T	ENSP00000495222.1:n.1593+13C>T
ENST00000647092.1:c.1257+13C>T	ENSP00000495176.1:n.1257+13C>T
ENST00000224721.10:c.7675+13C>T	ENSP00000224721.8:n.7675+13C>T
ENST00000398788.4:c.940+13C>T	ENSP00000381768.3:n.940+13C>T
ENST00000475158.1:n.1196+13C>T
ENST00000619887.4:c.940+13C>T	ENSP00000478374.1:n.940+13C>T
ENST00000622827.4:c.7660+13C>T	ENSP00000483211.1:n.7660+13C>T
NM_001171933.1:c.940+13C>T	NP_001165404.1:n.940+13C>T
NM_001171934.1:c.940+13C>T	NP_001165405.1:n.940+13C>T
NM_022124.5:c.7660+13C>T	NP_071407.4:n.7660+13C>T
XM_006717940.2:c.7855+13C>T	XP_006718003.1:n.7855+13C>T
XM_006717942.2:c.7789+13C>T	XP_006718005.1:n.7789+13C>T
XM_011540039.1:c.7852+13C>T	XP_011538341.1:n.7852+13C>T
XM_011540040.1:c.7849+13C>T	XP_011538342.1:n.7849+13C>T
XM_011540041.1:c.7795+13C>T	XP_011538343.1:n.7795+13C>T
XM_011540042.1:c.7765+13C>T	XP_011538344.1:n.7765+13C>T
XM_011540043.1:c.7855+13C>T	XP_011538345.1:n.7855+13C>T
XM_011540044.1:c.7720+13C>T	XP_011538346.1:n.7720+13C>T
XM_011540045.1:c.7855+13C>T	XP_011538347.1:n.7855+13C>T
XM_011540046.1:c.7315+13C>T	XP_011538348.1:n.7315+13C>T
XM_011540047.1:c.6673+13C>T	XP_011538349.1:n.6673+13C>T
XM_011540052.1:c.4183+13C>T	XP_011538354.1:n.4183+13C>T
NM_022124.6:c.7660+13C>T MANE Select	NP_071407.4:n.7660+13C>T