Canonical Allele Identifier: CA1918874262
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71793325G= , CM000672.2:g.71793325G= GRCh38
NC_000010.10:g.73553082G= , CM000672.1:g.73553082G= GRCh37
NC_000010.9:g.73223088G= NCBI36
NG_008835.1:g.401379G=

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.6397G= MANE Select ENSP00000224721.9:p.Asp2133=
ENST00000224721.10:c.6412G= ENSP00000224721.8:p.Asp2138=
ENST00000622827.4:c.6397G= ENSP00000483211.1:p.Asp2133=
NM_022124.5:c.6397G= NP_071407.4:p.Asp2133=
XM_006717940.2:c.6592G= XP_006718003.1:p.Asp2198=
XM_006717942.2:c.6526G= XP_006718005.1:p.Asp2176=
XM_011540039.1:c.6589G= XP_011538341.1:p.Asp2197=
XM_011540040.1:c.6586G= XP_011538342.1:p.Asp2196=
XM_011540041.1:c.6532G= XP_011538343.1:p.Asp2178=
XM_011540042.1:c.6577+15G= XP_011538344.1:n.6577+15G=
XM_011540043.1:c.6592G= XP_011538345.1:p.Asp2198=
XM_011540044.1:c.6457G= XP_011538346.1:p.Asp2153=
XM_011540045.1:c.6592G= XP_011538347.1:p.Asp2198=
XM_011540046.1:c.6052G= XP_011538348.1:p.Asp2018=
XM_011540047.1:c.5410G= XP_011538349.1:p.Asp1804=
XM_011540048.1:c.6592G= XP_011538350.1:p.Asp2198=
XM_011540049.1:c.6592G= XP_011538351.1:p.Asp2198=
XM_011540050.1:c.6592G= XP_011538352.1:p.Asp2198=
XM_011540051.1:c.6592G= XP_011538353.1:p.Asp2198=
XM_011540052.1:c.2920G= XP_011538354.1:p.Asp974=
XR_945796.1:n.6835G=
NM_022124.6:c.6397G= MANE Select NP_071407.4:p.Asp2133=