Canonical Allele Identifier: CA1918874200
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71793271C= , CM000672.2:g.71793271C= GRCh38
NC_000010.10:g.73553028C= , CM000672.1:g.73553028C= GRCh37
NC_000010.9:g.73223034C= NCBI36
NG_008835.1:g.401325C=

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.6343C= MANE Select ENSP00000224721.9:p.Arg2115=
ENST00000224721.10:c.6358C= ENSP00000224721.8:p.Arg2120=
ENST00000622827.4:c.6343C= ENSP00000483211.1:p.Arg2115=
NM_022124.5:c.6343C= NP_071407.4:p.Arg2115=
XM_006717940.2:c.6538C= XP_006718003.1:p.Arg2180=
XM_006717942.2:c.6472C= XP_006718005.1:p.Arg2158=
XM_011540039.1:c.6535C= XP_011538341.1:p.Arg2179=
XM_011540040.1:c.6532C= XP_011538342.1:p.Arg2178=
XM_011540041.1:c.6478C= XP_011538343.1:p.Arg2160=
XM_011540042.1:c.6538C= XP_011538344.1:p.Arg2180=
XM_011540043.1:c.6538C= XP_011538345.1:p.Arg2180=
XM_011540044.1:c.6403C= XP_011538346.1:p.Arg2135=
XM_011540045.1:c.6538C= XP_011538347.1:p.Arg2180=
XM_011540046.1:c.5998C= XP_011538348.1:p.Arg2000=
XM_011540047.1:c.5356C= XP_011538349.1:p.Arg1786=
XM_011540048.1:c.6538C= XP_011538350.1:p.Arg2180=
XM_011540049.1:c.6538C= XP_011538351.1:p.Arg2180=
XM_011540050.1:c.6538C= XP_011538352.1:p.Arg2180=
XM_011540051.1:c.6538C= XP_011538353.1:p.Arg2180=
XM_011540052.1:c.2866C= XP_011538354.1:p.Arg956=
XR_945796.1:n.6781C=
NM_022124.6:c.6343C= MANE Select NP_071407.4:p.Arg2115=