Canonical Allele Identifier: CA377146744
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71784994T>A , CM000672.2:g.71784994T>A GRCh38
NC_000010.10:g.73544751T>A , CM000672.1:g.73544751T>A GRCh37
NC_000010.9:g.73214757T>A NCBI36
NG_008835.1:g.393048T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.5606T>A MANE Select ENSP00000224721.9:p.Phe1869Tyr
ENST00000224721.10:c.5621T>A ENSP00000224721.8:p.Phe1874Tyr
ENST00000622827.4:c.5606T>A ENSP00000483211.1:p.Phe1869Tyr
NM_022124.5:c.5606T>A NP_071407.4:p.Phe1869Tyr
XM_006717940.2:c.5801T>A XP_006718003.1:p.Phe1934Tyr
XM_006717942.2:c.5735T>A XP_006718005.1:p.Phe1912Tyr
XM_011540039.1:c.5798T>A XP_011538341.1:p.Phe1933Tyr
XM_011540040.1:c.5795T>A XP_011538342.1:p.Phe1932Tyr
XM_011540041.1:c.5741T>A XP_011538343.1:p.Phe1914Tyr
XM_011540042.1:c.5801T>A XP_011538344.1:p.Phe1934Tyr
XM_011540043.1:c.5801T>A XP_011538345.1:p.Phe1934Tyr
XM_011540044.1:c.5666T>A XP_011538346.1:p.Phe1889Tyr
XM_011540045.1:c.5801T>A XP_011538347.1:p.Phe1934Tyr
XM_011540046.1:c.5261T>A XP_011538348.1:p.Phe1754Tyr
XM_011540047.1:c.4619T>A XP_011538349.1:p.Phe1540Tyr
XM_011540048.1:c.5801T>A XP_011538350.1:p.Phe1934Tyr
XM_011540049.1:c.5801T>A XP_011538351.1:p.Phe1934Tyr
XM_011540050.1:c.5801T>A XP_011538352.1:p.Phe1934Tyr
XM_011540051.1:c.5801T>A XP_011538353.1:p.Phe1934Tyr
XM_011540052.1:c.2129T>A XP_011538354.1:p.Phe710Tyr
XM_011540053.1:c.5801T>A XP_011538355.1:p.Phe1934Tyr
XR_945796.1:n.6044T>A
NM_022124.6:c.5606T>A MANE Select NP_071407.4:p.Phe1869Tyr