Canonical Allele Identifier: CA377143061
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71709119T>C , CM000672.2:g.71709119T>C GRCh38
NC_000010.10:g.73468876T>C , CM000672.1:g.73468876T>C GRCh37
NC_000010.9:g.73138882T>C NCBI36
NG_008835.1:g.317173T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.3128T>C MANE Select ENSP00000224721.9:p.Phe1043Ser
ENST00000398809.9:c.3128T>C ENSP00000381789.5:p.Phe1043Ser
ENST00000442677.4:c.3128T>C ENSP00000388894.3:p.Phe1043Ser
ENST00000466757.8:c.2559T>C
ENST00000224721.10:c.3143T>C ENSP00000224721.8:p.Phe1048Ser
ENST00000398809.8:c.3128T>C ENSP00000381789.5:p.Phe1043Ser
ENST00000442677.3:c.1903T>C
ENST00000466757.7:c.2559T>C
ENST00000616684.4:c.3128T>C ENSP00000482036.2:p.Phe1043Ser
ENST00000622827.4:c.3128T>C ENSP00000483211.1:p.Phe1043Ser
NM_001171930.1:c.3128T>C NP_001165401.1:p.Phe1043Ser
NM_022124.5:c.3128T>C NP_071407.4:p.Phe1043Ser
XM_006717940.2:c.3323T>C XP_006718003.1:p.Phe1108Ser
XM_006717942.2:c.3257T>C XP_006718005.1:p.Phe1086Ser
XM_011540039.1:c.3323T>C XP_011538341.1:p.Phe1108Ser
XM_011540040.1:c.3317T>C XP_011538342.1:p.Phe1106Ser
XM_011540041.1:c.3263T>C XP_011538343.1:p.Phe1088Ser
XM_011540042.1:c.3323T>C XP_011538344.1:p.Phe1108Ser
XM_011540043.1:c.3323T>C XP_011538345.1:p.Phe1108Ser
XM_011540044.1:c.3188T>C XP_011538346.1:p.Phe1063Ser
XM_011540045.1:c.3323T>C XP_011538347.1:p.Phe1108Ser
XM_011540046.1:c.2783T>C XP_011538348.1:p.Phe928Ser
XM_011540047.1:c.2141T>C XP_011538349.1:p.Phe714Ser
XM_011540048.1:c.3323T>C XP_011538350.1:p.Phe1108Ser
XM_011540049.1:c.3323T>C XP_011538351.1:p.Phe1108Ser
XM_011540050.1:c.3323T>C XP_011538352.1:p.Phe1108Ser
XM_011540051.1:c.3323T>C XP_011538353.1:p.Phe1108Ser
XM_011540053.1:c.3323T>C XP_011538355.1:p.Phe1108Ser
XR_945796.1:n.3566T>C
NM_001171930.2:c.3128T>C NP_001165401.1:p.Phe1043Ser
NM_022124.6:c.3128T>C MANE Select NP_071407.4:p.Phe1043Ser