Canonical Allele Identifier: CA377147032
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71785051T>G , CM000672.2:g.71785051T>G GRCh38
NC_000010.10:g.73544808T>G , CM000672.1:g.73544808T>G GRCh37
NC_000010.9:g.73214814T>G NCBI36
NG_008835.1:g.393105T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.5663T>G MANE Select ENSP00000224721.9:p.Phe1888Cys
ENST00000224721.10:c.5678T>G ENSP00000224721.8:p.Phe1893Cys
ENST00000622827.4:c.5663T>G ENSP00000483211.1:p.Phe1888Cys
NM_022124.5:c.5663T>G NP_071407.4:p.Phe1888Cys
XM_006717940.2:c.5858T>G XP_006718003.1:p.Phe1953Cys
XM_006717942.2:c.5792T>G XP_006718005.1:p.Phe1931Cys
XM_011540039.1:c.5855T>G XP_011538341.1:p.Phe1952Cys
XM_011540040.1:c.5852T>G XP_011538342.1:p.Phe1951Cys
XM_011540041.1:c.5798T>G XP_011538343.1:p.Phe1933Cys
XM_011540042.1:c.5858T>G XP_011538344.1:p.Phe1953Cys
XM_011540043.1:c.5858T>G XP_011538345.1:p.Phe1953Cys
XM_011540044.1:c.5723T>G XP_011538346.1:p.Phe1908Cys
XM_011540045.1:c.5858T>G XP_011538347.1:p.Phe1953Cys
XM_011540046.1:c.5318T>G XP_011538348.1:p.Phe1773Cys
XM_011540047.1:c.4676T>G XP_011538349.1:p.Phe1559Cys
XM_011540048.1:c.5858T>G XP_011538350.1:p.Phe1953Cys
XM_011540049.1:c.5858T>G XP_011538351.1:p.Phe1953Cys
XM_011540050.1:c.5858T>G XP_011538352.1:p.Phe1953Cys
XM_011540051.1:c.5858T>G XP_011538353.1:p.Phe1953Cys
XM_011540052.1:c.2186T>G XP_011538354.1:p.Phe729Cys
XM_011540053.1:c.5858T>G XP_011538355.1:p.Phe1953Cys
XR_945796.1:n.6101T>G
NM_022124.6:c.5663T>G MANE Select NP_071407.4:p.Phe1888Cys