Canonical Allele Identifier: CA5545823
Gene: CDH23 HGNC NCBI

Linked Data

dbSNP Id: rs528110026

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71785034C>G , CM000672.2:g.71785034C>G GRCh38
NC_000010.10:g.73544791C>G , CM000672.1:g.73544791C>G GRCh37
NC_000010.9:g.73214797C>G NCBI36
NG_008835.1:g.393088C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.5646C>G MANE Select ENSP00000224721.9:p.Cys1882Trp
ENST00000224721.10:c.5661C>G ENSP00000224721.8:p.Cys1887Trp
ENST00000622827.4:c.5646C>G ENSP00000483211.1:p.Cys1882Trp
NM_022124.5:c.5646C>G NP_071407.4:p.Cys1882Trp
XM_006717940.2:c.5841C>G XP_006718003.1:p.Cys1947Trp
XM_006717942.2:c.5775C>G XP_006718005.1:p.Cys1925Trp
XM_011540039.1:c.5838C>G XP_011538341.1:p.Cys1946Trp
XM_011540040.1:c.5835C>G XP_011538342.1:p.Cys1945Trp
XM_011540041.1:c.5781C>G XP_011538343.1:p.Cys1927Trp
XM_011540042.1:c.5841C>G XP_011538344.1:p.Cys1947Trp
XM_011540043.1:c.5841C>G XP_011538345.1:p.Cys1947Trp
XM_011540044.1:c.5706C>G XP_011538346.1:p.Cys1902Trp
XM_011540045.1:c.5841C>G XP_011538347.1:p.Cys1947Trp
XM_011540046.1:c.5301C>G XP_011538348.1:p.Cys1767Trp
XM_011540047.1:c.4659C>G XP_011538349.1:p.Cys1553Trp
XM_011540048.1:c.5841C>G XP_011538350.1:p.Cys1947Trp
XM_011540049.1:c.5841C>G XP_011538351.1:p.Cys1947Trp
XM_011540050.1:c.5841C>G XP_011538352.1:p.Cys1947Trp
XM_011540051.1:c.5841C>G XP_011538353.1:p.Cys1947Trp
XM_011540052.1:c.2169C>G XP_011538354.1:p.Cys723Trp
XM_011540053.1:c.5841C>G XP_011538355.1:p.Cys1947Trp
XR_945796.1:n.6084C>G
NM_022124.6:c.5646C>G MANE Select NP_071407.4:p.Cys1882Trp