Canonical Allele Identifier: CA377147018
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71785047A>C , CM000672.2:g.71785047A>C GRCh38
NC_000010.10:g.73544804A>C , CM000672.1:g.73544804A>C GRCh37
NC_000010.9:g.73214810A>C NCBI36
NG_008835.1:g.393101A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.5659A>C MANE Select ENSP00000224721.9:p.Thr1887Pro
ENST00000224721.10:c.5674A>C ENSP00000224721.8:p.Thr1892Pro
ENST00000622827.4:c.5659A>C ENSP00000483211.1:p.Thr1887Pro
NM_022124.5:c.5659A>C NP_071407.4:p.Thr1887Pro
XM_006717940.2:c.5854A>C XP_006718003.1:p.Thr1952Pro
XM_006717942.2:c.5788A>C XP_006718005.1:p.Thr1930Pro
XM_011540039.1:c.5851A>C XP_011538341.1:p.Thr1951Pro
XM_011540040.1:c.5848A>C XP_011538342.1:p.Thr1950Pro
XM_011540041.1:c.5794A>C XP_011538343.1:p.Thr1932Pro
XM_011540042.1:c.5854A>C XP_011538344.1:p.Thr1952Pro
XM_011540043.1:c.5854A>C XP_011538345.1:p.Thr1952Pro
XM_011540044.1:c.5719A>C XP_011538346.1:p.Thr1907Pro
XM_011540045.1:c.5854A>C XP_011538347.1:p.Thr1952Pro
XM_011540046.1:c.5314A>C XP_011538348.1:p.Thr1772Pro
XM_011540047.1:c.4672A>C XP_011538349.1:p.Thr1558Pro
XM_011540048.1:c.5854A>C XP_011538350.1:p.Thr1952Pro
XM_011540049.1:c.5854A>C XP_011538351.1:p.Thr1952Pro
XM_011540050.1:c.5854A>C XP_011538352.1:p.Thr1952Pro
XM_011540051.1:c.5854A>C XP_011538353.1:p.Thr1952Pro
XM_011540052.1:c.2182A>C XP_011538354.1:p.Thr728Pro
XM_011540053.1:c.5854A>C XP_011538355.1:p.Thr1952Pro
XR_945796.1:n.6097A>C
NM_022124.6:c.5659A>C MANE Select NP_071407.4:p.Thr1887Pro