Canonical Allele Identifier: CA377160344
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71740836C>A , CM000672.2:g.71740836C>A GRCh38
NC_000010.10:g.73500593C>A , CM000672.1:g.73500593C>A GRCh37
NC_000010.9:g.73170599C>A NCBI36
NG_008835.1:g.348890C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.4503C>A MANE Select ENSP00000224721.9:p.Asp1501Glu
ENST00000224721.10:c.4518C>A ENSP00000224721.8:p.Asp1506Glu
ENST00000398792.3:n.1192C>A
ENST00000622827.4:c.4503C>A ENSP00000483211.1:p.Asp1501Glu
NM_022124.5:c.4503C>A NP_071407.4:p.Asp1501Glu
XM_006717940.2:c.4698C>A XP_006718003.1:p.Asp1566Glu
XM_006717942.2:c.4632C>A XP_006718005.1:p.Asp1544Glu
XM_011540039.1:c.4695C>A XP_011538341.1:p.Asp1565Glu
XM_011540040.1:c.4692C>A XP_011538342.1:p.Asp1564Glu
XM_011540041.1:c.4638C>A XP_011538343.1:p.Asp1546Glu
XM_011540042.1:c.4698C>A XP_011538344.1:p.Asp1566Glu
XM_011540043.1:c.4698C>A XP_011538345.1:p.Asp1566Glu
XM_011540044.1:c.4563C>A XP_011538346.1:p.Asp1521Glu
XM_011540045.1:c.4698C>A XP_011538347.1:p.Asp1566Glu
XM_011540046.1:c.4158C>A XP_011538348.1:p.Asp1386Glu
XM_011540047.1:c.3516C>A XP_011538349.1:p.Asp1172Glu
XM_011540048.1:c.4698C>A XP_011538350.1:p.Asp1566Glu
XM_011540049.1:c.4698C>A XP_011538351.1:p.Asp1566Glu
XM_011540050.1:c.4698C>A XP_011538352.1:p.Asp1566Glu
XM_011540051.1:c.4698C>A XP_011538353.1:p.Asp1566Glu
XM_011540052.1:c.1026C>A XP_011538354.1:p.Asp342Glu
XM_011540053.1:c.4698C>A XP_011538355.1:p.Asp1566Glu
XR_945796.1:n.4941C>A
NM_022124.6:c.4503C>A MANE Select NP_071407.4:p.Asp1501Glu