Canonical Allele Identifier: CA1918878362
Gene: CDH23 HGNC NCBI

Linked Data

dbSNP Id: rs1589427806

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71798300G>C , CM000672.2:g.71798300G>C GRCh38
NC_000010.10:g.73558057G>C , CM000672.1:g.73558057G>C GRCh37
NC_000010.9:g.73228063G>C NCBI36
NG_008835.1:g.406354G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.6830-54G>C MANE Select ENSP00000224721.9:n.6830-54G>C
ENST00000642965.1:c.763-54G>C ENSP00000495222.1:n.763-54G>C
ENST00000647092.1:c.427-54G>C ENSP00000495176.1:n.427-54G>C
ENST00000224721.10:c.6845-54G>C ENSP00000224721.8:n.6845-54G>C
ENST00000398788.4:c.110-54G>C ENSP00000381768.3:n.110-54G>C
ENST00000475158.1:n.366-54G>C
ENST00000619887.4:c.110-54G>C ENSP00000478374.1:n.110-54G>C
ENST00000622827.4:c.6830-54G>C ENSP00000483211.1:n.6830-54G>C
NM_001171933.1:c.110-54G>C NP_001165404.1:n.110-54G>C
NM_001171934.1:c.110-54G>C NP_001165405.1:n.110-54G>C
NM_022124.5:c.6830-54G>C NP_071407.4:n.6830-54G>C
XM_006717940.2:c.7025-54G>C XP_006718003.1:n.7025-54G>C
XM_006717942.2:c.6959-54G>C XP_006718005.1:n.6959-54G>C
XM_011540039.1:c.7022-54G>C XP_011538341.1:n.7022-54G>C
XM_011540040.1:c.7019-54G>C XP_011538342.1:n.7019-54G>C
XM_011540041.1:c.6965-54G>C XP_011538343.1:n.6965-54G>C
XM_011540042.1:c.6935-54G>C XP_011538344.1:n.6935-54G>C
XM_011540043.1:c.7025-54G>C XP_011538345.1:n.7025-54G>C
XM_011540044.1:c.6890-54G>C XP_011538346.1:n.6890-54G>C
XM_011540045.1:c.7025-54G>C XP_011538347.1:n.7025-54G>C
XM_011540046.1:c.6485-54G>C XP_011538348.1:n.6485-54G>C
XM_011540047.1:c.5843-54G>C XP_011538349.1:n.5843-54G>C
XM_011540052.1:c.3353-54G>C XP_011538354.1:n.3353-54G>C
NM_022124.6:c.6830-54G>C MANE Select NP_071407.4:n.6830-54G>C