Canonical Allele Identifier: CA1918874458
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71793420C= , CM000672.2:g.71793420C= GRCh38
NC_000010.10:g.73553177C= , CM000672.1:g.73553177C= GRCh37
NC_000010.9:g.73223183C= NCBI36
NG_008835.1:g.401474C=

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.6492C= MANE Select ENSP00000224721.9:p.Ile2164=
ENST00000224721.10:c.6507C= ENSP00000224721.8:p.Ile2169=
ENST00000622827.4:c.6492C= ENSP00000483211.1:p.Ile2164=
NM_022124.5:c.6492C= NP_071407.4:p.Ile2164=
XM_006717940.2:c.6687C= XP_006718003.1:p.Ile2229=
XM_006717942.2:c.6621C= XP_006718005.1:p.Ile2207=
XM_011540039.1:c.6684C= XP_011538341.1:p.Ile2228=
XM_011540040.1:c.6681C= XP_011538342.1:p.Ile2227=
XM_011540041.1:c.6627C= XP_011538343.1:p.Ile2209=
XM_011540042.1:c.6597C= XP_011538344.1:p.Ile2199=
XM_011540043.1:c.6687C= XP_011538345.1:p.Ile2229=
XM_011540044.1:c.6552C= XP_011538346.1:p.Ile2184=
XM_011540045.1:c.6687C= XP_011538347.1:p.Ile2229=
XM_011540046.1:c.6147C= XP_011538348.1:p.Ile2049=
XM_011540047.1:c.5505C= XP_011538349.1:p.Ile1835=
XM_011540048.1:c.6687C= XP_011538350.1:p.Ile2229=
XM_011540049.1:c.6687C= XP_011538351.1:p.Ile2229=
XM_011540050.1:c.6687C= XP_011538352.1:p.Ile2229=
XM_011540051.1:c.6687C= XP_011538353.1:p.Ile2229=
XM_011540052.1:c.3015C= XP_011538354.1:p.Ile1005=
XR_945796.1:n.6930C=
NM_022124.6:c.6492C= MANE Select NP_071407.4:p.Ile2164=