Canonical Allele Identifier: CA1918861775
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71784786A= , CM000672.2:g.71784786A= GRCh38
NC_000010.10:g.73544543A= , CM000672.1:g.73544543A= GRCh37
NC_000010.9:g.73214549A= NCBI36
NG_008835.1:g.392840A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.5503-105A= MANE Select ENSP00000224721.9:n.5503-105A=
ENST00000224721.10:c.5518-105A= ENSP00000224721.8:n.5518-105A=
ENST00000622827.4:c.5503-105A= ENSP00000483211.1:n.5503-105A=
NM_022124.5:c.5503-105A= NP_071407.4:n.5503-105A=
XM_006717940.2:c.5698-105A= XP_006718003.1:n.5698-105A=
XM_006717942.2:c.5632-105A= XP_006718005.1:n.5632-105A=
XM_011540039.1:c.5695-105A= XP_011538341.1:n.5695-105A=
XM_011540040.1:c.5692-105A= XP_011538342.1:n.5692-105A=
XM_011540041.1:c.5638-105A= XP_011538343.1:n.5638-105A=
XM_011540042.1:c.5698-105A= XP_011538344.1:n.5698-105A=
XM_011540043.1:c.5698-105A= XP_011538345.1:n.5698-105A=
XM_011540044.1:c.5563-105A= XP_011538346.1:n.5563-105A=
XM_011540045.1:c.5698-105A= XP_011538347.1:n.5698-105A=
XM_011540046.1:c.5158-105A= XP_011538348.1:n.5158-105A=
XM_011540047.1:c.4516-105A= XP_011538349.1:n.4516-105A=
XM_011540048.1:c.5698-105A= XP_011538350.1:n.5698-105A=
XM_011540049.1:c.5698-105A= XP_011538351.1:n.5698-105A=
XM_011540050.1:c.5698-105A= XP_011538352.1:n.5698-105A=
XM_011540051.1:c.5698-105A= XP_011538353.1:n.5698-105A=
XM_011540052.1:c.2026-105A= XP_011538354.1:n.2026-105A=
XM_011540053.1:c.5698-105A= XP_011538355.1:n.5698-105A=
XR_945796.1:n.5941-105A=
NM_022124.6:c.5503-105A= MANE Select NP_071407.4:n.5503-105A=