Canonical Allele Identifier: CA2609580508

Gene: CDH23

Linked Data

• gnomAD v4: 10-71803103-A-ATTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71803104_71803105insTTTT , CM000672.2:g.71803104_71803105insTTTT	GRCh38
NC_000010.10:g.73562861_73562862insTTTT , CM000672.1:g.73562861_73562862insTTTT	GRCh37
NC_000010.9:g.73232867_73232868insTTTT	NCBI36
NG_008835.1:g.411158_411159insTTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7660+29_7660+30insTTTT MANE Select	ENSP00000224721.9:n.7660+29_7660+30insTTT...
ENST00000642965.1:c.1593+29_1593+30insTTTT	ENSP00000495222.1:n.1593+29_1593+30insTTT...
ENST00000647092.1:c.1257+29_1257+30insTTTT	ENSP00000495176.1:n.1257+29_1257+30insTTT...
ENST00000224721.10:c.7675+29_7675+30insTTTT	ENSP00000224721.8:n.7675+29_7675+30insTTT...
ENST00000398788.4:c.940+29_940+30insTTTT	ENSP00000381768.3:n.940+29_940+30insTTTT
ENST00000475158.1:n.1196+29_1196+30insTTTT
ENST00000619887.4:c.940+29_940+30insTTTT	ENSP00000478374.1:n.940+29_940+30insTTTT
ENST00000622827.4:c.7660+29_7660+30insTTTT	ENSP00000483211.1:n.7660+29_7660+30insTTT...
NM_001171933.1:c.940+29_940+30insTTTT	NP_001165404.1:n.940+29_940+30insTTTT
NM_001171934.1:c.940+29_940+30insTTTT	NP_001165405.1:n.940+29_940+30insTTTT
NM_022124.5:c.7660+29_7660+30insTTTT	NP_071407.4:n.7660+29_7660+30insTTTT
XM_006717940.2:c.7855+29_7855+30insTTTT	XP_006718003.1:n.7855+29_7855+30insTTTT
XM_006717942.2:c.7789+29_7789+30insTTTT	XP_006718005.1:n.7789+29_7789+30insTTTT
XM_011540039.1:c.7852+29_7852+30insTTTT	XP_011538341.1:n.7852+29_7852+30insTTTT
XM_011540040.1:c.7849+29_7849+30insTTTT	XP_011538342.1:n.7849+29_7849+30insTTTT
XM_011540041.1:c.7795+29_7795+30insTTTT	XP_011538343.1:n.7795+29_7795+30insTTTT
XM_011540042.1:c.7765+29_7765+30insTTTT	XP_011538344.1:n.7765+29_7765+30insTTTT
XM_011540043.1:c.7855+29_7855+30insTTTT	XP_011538345.1:n.7855+29_7855+30insTTTT
XM_011540044.1:c.7720+29_7720+30insTTTT	XP_011538346.1:n.7720+29_7720+30insTTTT
XM_011540045.1:c.7855+29_7855+30insTTTT	XP_011538347.1:n.7855+29_7855+30insTTTT
XM_011540046.1:c.7315+29_7315+30insTTTT	XP_011538348.1:n.7315+29_7315+30insTTTT
XM_011540047.1:c.6673+29_6673+30insTTTT	XP_011538349.1:n.6673+29_6673+30insTTTT
XM_011540052.1:c.4183+29_4183+30insTTTT	XP_011538354.1:n.4183+29_4183+30insTTTT
NM_022124.6:c.7660+29_7660+30insTTTT MANE Select	NP_071407.4:n.7660+29_7660+30insTTTT