Canonical Allele Identifier: CA1918870161
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71790323G= , CM000672.2:g.71790323G= GRCh38
NC_000010.10:g.73550080G= , CM000672.1:g.73550080G= GRCh37
NC_000010.9:g.73220086G= NCBI36
NG_008835.1:g.398377G=

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.5959G= MANE Select ENSP00000224721.9:p.Ala1987=
ENST00000224721.10:c.5974G= ENSP00000224721.8:p.Ala1992=
ENST00000622827.4:c.5959G= ENSP00000483211.1:p.Ala1987=
NM_022124.5:c.5959G= NP_071407.4:p.Ala1987=
XM_006717940.2:c.6154G= XP_006718003.1:p.Ala2052=
XM_006717942.2:c.6088G= XP_006718005.1:p.Ala2030=
XM_011540039.1:c.6151G= XP_011538341.1:p.Ala2051=
XM_011540040.1:c.6148G= XP_011538342.1:p.Ala2050=
XM_011540041.1:c.6094G= XP_011538343.1:p.Ala2032=
XM_011540042.1:c.6154G= XP_011538344.1:p.Ala2052=
XM_011540043.1:c.6154G= XP_011538345.1:p.Ala2052=
XM_011540044.1:c.6019G= XP_011538346.1:p.Ala2007=
XM_011540045.1:c.6154G= XP_011538347.1:p.Ala2052=
XM_011540046.1:c.5614G= XP_011538348.1:p.Ala1872=
XM_011540047.1:c.4972G= XP_011538349.1:p.Ala1658=
XM_011540048.1:c.6154G= XP_011538350.1:p.Ala2052=
XM_011540049.1:c.6154G= XP_011538351.1:p.Ala2052=
XM_011540050.1:c.6154G= XP_011538352.1:p.Ala2052=
XM_011540051.1:c.6154G= XP_011538353.1:p.Ala2052=
XM_011540052.1:c.2482G= XP_011538354.1:p.Ala828=
XR_945796.1:n.6397G=
NM_022124.6:c.5959G= MANE Select NP_071407.4:p.Ala1987=