Canonical Allele Identifier: CA1918862344
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71785006T= , CM000672.2:g.71785006T= GRCh38
NC_000010.10:g.73544763T= , CM000672.1:g.73544763T= GRCh37
NC_000010.9:g.73214769T= NCBI36
NG_008835.1:g.393060T=

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.5618T= MANE Select ENSP00000224721.9:p.Val1873=
ENST00000224721.10:c.5633T= ENSP00000224721.8:p.Val1878=
ENST00000622827.4:c.5618T= ENSP00000483211.1:p.Val1873=
NM_022124.5:c.5618T= NP_071407.4:p.Val1873=
XM_006717940.2:c.5813T= XP_006718003.1:p.Val1938=
XM_006717942.2:c.5747T= XP_006718005.1:p.Val1916=
XM_011540039.1:c.5810T= XP_011538341.1:p.Val1937=
XM_011540040.1:c.5807T= XP_011538342.1:p.Val1936=
XM_011540041.1:c.5753T= XP_011538343.1:p.Val1918=
XM_011540042.1:c.5813T= XP_011538344.1:p.Val1938=
XM_011540043.1:c.5813T= XP_011538345.1:p.Val1938=
XM_011540044.1:c.5678T= XP_011538346.1:p.Val1893=
XM_011540045.1:c.5813T= XP_011538347.1:p.Val1938=
XM_011540046.1:c.5273T= XP_011538348.1:p.Val1758=
XM_011540047.1:c.4631T= XP_011538349.1:p.Val1544=
XM_011540048.1:c.5813T= XP_011538350.1:p.Val1938=
XM_011540049.1:c.5813T= XP_011538351.1:p.Val1938=
XM_011540050.1:c.5813T= XP_011538352.1:p.Val1938=
XM_011540051.1:c.5813T= XP_011538353.1:p.Val1938=
XM_011540052.1:c.2141T= XP_011538354.1:p.Val714=
XM_011540053.1:c.5813T= XP_011538355.1:p.Val1938=
XR_945796.1:n.6056T=
NM_022124.6:c.5618T= MANE Select NP_071407.4:p.Val1873=