Canonical Allele Identifier: CA2788480130
Gene: CDH23 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71784208A>C , CM000672.2:g.71784208A>C GRCh38
NC_000010.10:g.73543965A>C , CM000672.1:g.73543965A>C GRCh37
NC_000010.9:g.73213971A>C NCBI36
NG_008835.1:g.392262A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.5369-79A>C MANE Select ENSP00000224721.9:n.5369-79A>C
ENST00000224721.10:c.5384-79A>C ENSP00000224721.8:n.5384-79A>C
ENST00000622827.4:c.5369-79A>C ENSP00000483211.1:n.5369-79A>C
NM_022124.5:c.5369-79A>C NP_071407.4:n.5369-79A>C
XM_006717940.2:c.5564-79A>C XP_006718003.1:n.5564-79A>C
XM_006717942.2:c.5498-79A>C XP_006718005.1:n.5498-79A>C
XM_011540039.1:c.5561-79A>C XP_011538341.1:n.5561-79A>C
XM_011540040.1:c.5558-79A>C XP_011538342.1:n.5558-79A>C
XM_011540041.1:c.5504-79A>C XP_011538343.1:n.5504-79A>C
XM_011540042.1:c.5564-79A>C XP_011538344.1:n.5564-79A>C
XM_011540043.1:c.5564-79A>C XP_011538345.1:n.5564-79A>C
XM_011540044.1:c.5429-79A>C XP_011538346.1:n.5429-79A>C
XM_011540045.1:c.5564-79A>C XP_011538347.1:n.5564-79A>C
XM_011540046.1:c.5024-79A>C XP_011538348.1:n.5024-79A>C
XM_011540047.1:c.4382-79A>C XP_011538349.1:n.4382-79A>C
XM_011540048.1:c.5564-79A>C XP_011538350.1:n.5564-79A>C
XM_011540049.1:c.5564-79A>C XP_011538351.1:n.5564-79A>C
XM_011540050.1:c.5564-79A>C XP_011538352.1:n.5564-79A>C
XM_011540051.1:c.5564-79A>C XP_011538353.1:n.5564-79A>C
XM_011540052.1:c.1892-79A>C XP_011538354.1:n.1892-79A>C
XM_011540053.1:c.5564-79A>C XP_011538355.1:n.5564-79A>C
XR_945796.1:n.5807-79A>C
NM_022124.6:c.5369-79A>C MANE Select NP_071407.4:n.5369-79A>C
Search 100 bp 5'
Search 100 bp 3'