Canonical Allele Identifier: CA2697558464

Gene: CDH23

Linked Data

• ClinVar Variation Id: 2751375
• ClinVar RCV Id: RCV003570846

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71803094A>G , CM000672.2:g.71803094A>G	GRCh38
NC_000010.10:g.73562851A>G , CM000672.1:g.73562851A>G	GRCh37
NC_000010.9:g.73232857A>G	NCBI36
NG_008835.1:g.411148A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7660+19A>G MANE Select	ENSP00000224721.9:n.7660+19A>G
ENST00000642965.1:c.1593+19A>G	ENSP00000495222.1:n.1593+19A>G
ENST00000647092.1:c.1257+19A>G	ENSP00000495176.1:n.1257+19A>G
ENST00000224721.10:c.7675+19A>G	ENSP00000224721.8:n.7675+19A>G
ENST00000398788.4:c.940+19A>G	ENSP00000381768.3:n.940+19A>G
ENST00000475158.1:n.1196+19A>G
ENST00000619887.4:c.940+19A>G	ENSP00000478374.1:n.940+19A>G
ENST00000622827.4:c.7660+19A>G	ENSP00000483211.1:n.7660+19A>G
NM_001171933.1:c.940+19A>G	NP_001165404.1:n.940+19A>G
NM_001171934.1:c.940+19A>G	NP_001165405.1:n.940+19A>G
NM_022124.5:c.7660+19A>G	NP_071407.4:n.7660+19A>G
XM_006717940.2:c.7855+19A>G	XP_006718003.1:n.7855+19A>G
XM_006717942.2:c.7789+19A>G	XP_006718005.1:n.7789+19A>G
XM_011540039.1:c.7852+19A>G	XP_011538341.1:n.7852+19A>G
XM_011540040.1:c.7849+19A>G	XP_011538342.1:n.7849+19A>G
XM_011540041.1:c.7795+19A>G	XP_011538343.1:n.7795+19A>G
XM_011540042.1:c.7765+19A>G	XP_011538344.1:n.7765+19A>G
XM_011540043.1:c.7855+19A>G	XP_011538345.1:n.7855+19A>G
XM_011540044.1:c.7720+19A>G	XP_011538346.1:n.7720+19A>G
XM_011540045.1:c.7855+19A>G	XP_011538347.1:n.7855+19A>G
XM_011540046.1:c.7315+19A>G	XP_011538348.1:n.7315+19A>G
XM_011540047.1:c.6673+19A>G	XP_011538349.1:n.6673+19A>G
XM_011540052.1:c.4183+19A>G	XP_011538354.1:n.4183+19A>G
NM_022124.6:c.7660+19A>G MANE Select	NP_071407.4:n.7660+19A>G