Canonical Allele Identifier: CA1918870408
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71790413G= , CM000672.2:g.71790413G= GRCh38
NC_000010.10:g.73550170G= , CM000672.1:g.73550170G= GRCh37
NC_000010.9:g.73220176G= NCBI36
NG_008835.1:g.398467G=

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.6049G= MANE Select ENSP00000224721.9:p.Gly2017=
ENST00000224721.10:c.6064G= ENSP00000224721.8:p.Gly2022=
ENST00000622827.4:c.6049G= ENSP00000483211.1:p.Gly2017=
NM_022124.5:c.6049G= NP_071407.4:p.Gly2017=
XM_006717940.2:c.6244G= XP_006718003.1:p.Gly2082=
XM_006717942.2:c.6178G= XP_006718005.1:p.Gly2060=
XM_011540039.1:c.6241G= XP_011538341.1:p.Gly2081=
XM_011540040.1:c.6238G= XP_011538342.1:p.Gly2080=
XM_011540041.1:c.6184G= XP_011538343.1:p.Gly2062=
XM_011540042.1:c.6244G= XP_011538344.1:p.Gly2082=
XM_011540043.1:c.6244G= XP_011538345.1:p.Gly2082=
XM_011540044.1:c.6109G= XP_011538346.1:p.Gly2037=
XM_011540045.1:c.6244G= XP_011538347.1:p.Gly2082=
XM_011540046.1:c.5704G= XP_011538348.1:p.Gly1902=
XM_011540047.1:c.5062G= XP_011538349.1:p.Gly1688=
XM_011540048.1:c.6244G= XP_011538350.1:p.Gly2082=
XM_011540049.1:c.6244G= XP_011538351.1:p.Gly2082=
XM_011540050.1:c.6244G= XP_011538352.1:p.Gly2082=
XM_011540051.1:c.6244G= XP_011538353.1:p.Gly2082=
XM_011540052.1:c.2572G= XP_011538354.1:p.Gly858=
XR_945796.1:n.6487G=
NM_022124.6:c.6049G= MANE Select NP_071407.4:p.Gly2017=