Canonical Allele Identifier: CA1918874260
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71793324C= , CM000672.2:g.71793324C= GRCh38
NC_000010.10:g.73553081C= , CM000672.1:g.73553081C= GRCh37
NC_000010.9:g.73223087C= NCBI36
NG_008835.1:g.401378C=

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.6396C= MANE Select ENSP00000224721.9:p.Ile2132=
ENST00000224721.10:c.6411C= ENSP00000224721.8:p.Ile2137=
ENST00000622827.4:c.6396C= ENSP00000483211.1:p.Ile2132=
NM_022124.5:c.6396C= NP_071407.4:p.Ile2132=
XM_006717940.2:c.6591C= XP_006718003.1:p.Ile2197=
XM_006717942.2:c.6525C= XP_006718005.1:p.Ile2175=
XM_011540039.1:c.6588C= XP_011538341.1:p.Ile2196=
XM_011540040.1:c.6585C= XP_011538342.1:p.Ile2195=
XM_011540041.1:c.6531C= XP_011538343.1:p.Ile2177=
XM_011540042.1:c.6577+14C= XP_011538344.1:n.6577+14C=
XM_011540043.1:c.6591C= XP_011538345.1:p.Ile2197=
XM_011540044.1:c.6456C= XP_011538346.1:p.Ile2152=
XM_011540045.1:c.6591C= XP_011538347.1:p.Ile2197=
XM_011540046.1:c.6051C= XP_011538348.1:p.Ile2017=
XM_011540047.1:c.5409C= XP_011538349.1:p.Ile1803=
XM_011540048.1:c.6591C= XP_011538350.1:p.Ile2197=
XM_011540049.1:c.6591C= XP_011538351.1:p.Ile2197=
XM_011540050.1:c.6591C= XP_011538352.1:p.Ile2197=
XM_011540051.1:c.6591C= XP_011538353.1:p.Ile2197=
XM_011540052.1:c.2919C= XP_011538354.1:p.Ile973=
XR_945796.1:n.6834C=
NM_022124.6:c.6396C= MANE Select NP_071407.4:p.Ile2132=