Canonical Allele Identifier: CA377146801
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71785012C>A , CM000672.2:g.71785012C>A GRCh38
NC_000010.10:g.73544769C>A , CM000672.1:g.73544769C>A GRCh37
NC_000010.9:g.73214775C>A NCBI36
NG_008835.1:g.393066C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.5624C>A MANE Select ENSP00000224721.9:p.Ala1875Asp
ENST00000224721.10:c.5639C>A ENSP00000224721.8:p.Ala1880Asp
ENST00000622827.4:c.5624C>A ENSP00000483211.1:p.Ala1875Asp
NM_022124.5:c.5624C>A NP_071407.4:p.Ala1875Asp
XM_006717940.2:c.5819C>A XP_006718003.1:p.Ala1940Asp
XM_006717942.2:c.5753C>A XP_006718005.1:p.Ala1918Asp
XM_011540039.1:c.5816C>A XP_011538341.1:p.Ala1939Asp
XM_011540040.1:c.5813C>A XP_011538342.1:p.Ala1938Asp
XM_011540041.1:c.5759C>A XP_011538343.1:p.Ala1920Asp
XM_011540042.1:c.5819C>A XP_011538344.1:p.Ala1940Asp
XM_011540043.1:c.5819C>A XP_011538345.1:p.Ala1940Asp
XM_011540044.1:c.5684C>A XP_011538346.1:p.Ala1895Asp
XM_011540045.1:c.5819C>A XP_011538347.1:p.Ala1940Asp
XM_011540046.1:c.5279C>A XP_011538348.1:p.Ala1760Asp
XM_011540047.1:c.4637C>A XP_011538349.1:p.Ala1546Asp
XM_011540048.1:c.5819C>A XP_011538350.1:p.Ala1940Asp
XM_011540049.1:c.5819C>A XP_011538351.1:p.Ala1940Asp
XM_011540050.1:c.5819C>A XP_011538352.1:p.Ala1940Asp
XM_011540051.1:c.5819C>A XP_011538353.1:p.Ala1940Asp
XM_011540052.1:c.2147C>A XP_011538354.1:p.Ala716Asp
XM_011540053.1:c.5819C>A XP_011538355.1:p.Ala1940Asp
XR_945796.1:n.6062C>A
NM_022124.6:c.5624C>A MANE Select NP_071407.4:p.Ala1875Asp