Canonical Allele Identifier: CA2722285850
Gene: CDH23 HGNC NCBI

Linked Data

dbSNP Id: rs2132953637

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71793342G>A , CM000672.2:g.71793342G>A GRCh38
NC_000010.10:g.73553099G>A , CM000672.1:g.73553099G>A GRCh37
NC_000010.9:g.73223105G>A NCBI36
NG_008835.1:g.401396G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.6414G>A MANE Select ENSP00000224721.9:p.Glu2138=
ENST00000224721.10:c.6429G>A ENSP00000224721.8:p.Glu2143=
ENST00000622827.4:c.6414G>A ENSP00000483211.1:p.Glu2138=
NM_022124.5:c.6414G>A NP_071407.4:p.Glu2138=
XM_006717940.2:c.6609G>A XP_006718003.1:p.Glu2203=
XM_006717942.2:c.6543G>A XP_006718005.1:p.Glu2181=
XM_011540039.1:c.6606G>A XP_011538341.1:p.Glu2202=
XM_011540040.1:c.6603G>A XP_011538342.1:p.Glu2201=
XM_011540041.1:c.6549G>A XP_011538343.1:p.Glu2183=
XM_011540042.1:c.6577+32G>A XP_011538344.1:n.6577+32G>A
XM_011540043.1:c.6609G>A XP_011538345.1:p.Glu2203=
XM_011540044.1:c.6474G>A XP_011538346.1:p.Glu2158=
XM_011540045.1:c.6609G>A XP_011538347.1:p.Glu2203=
XM_011540046.1:c.6069G>A XP_011538348.1:p.Glu2023=
XM_011540047.1:c.5427G>A XP_011538349.1:p.Glu1809=
XM_011540048.1:c.6609G>A XP_011538350.1:p.Glu2203=
XM_011540049.1:c.6609G>A XP_011538351.1:p.Glu2203=
XM_011540050.1:c.6609G>A XP_011538352.1:p.Glu2203=
XM_011540051.1:c.6609G>A XP_011538353.1:p.Glu2203=
XM_011540052.1:c.2937G>A XP_011538354.1:p.Glu979=
XR_945796.1:n.6852G>A
NM_022124.6:c.6414G>A MANE Select NP_071407.4:p.Glu2138=