Canonical Allele Identifier: CA377154830
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71793332A>T , CM000672.2:g.71793332A>T GRCh38
NC_000010.10:g.73553089A>T , CM000672.1:g.73553089A>T GRCh37
NC_000010.9:g.73223095A>T NCBI36
NG_008835.1:g.401386A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.6404A>T MANE Select ENSP00000224721.9:p.Glu2135Val
ENST00000224721.10:c.6419A>T ENSP00000224721.8:p.Glu2140Val
ENST00000622827.4:c.6404A>T ENSP00000483211.1:p.Glu2135Val
NM_022124.5:c.6404A>T NP_071407.4:p.Glu2135Val
XM_006717940.2:c.6599A>T XP_006718003.1:p.Glu2200Val
XM_006717942.2:c.6533A>T XP_006718005.1:p.Glu2178Val
XM_011540039.1:c.6596A>T XP_011538341.1:p.Glu2199Val
XM_011540040.1:c.6593A>T XP_011538342.1:p.Glu2198Val
XM_011540041.1:c.6539A>T XP_011538343.1:p.Glu2180Val
XM_011540042.1:c.6577+22A>T XP_011538344.1:n.6577+22A>T
XM_011540043.1:c.6599A>T XP_011538345.1:p.Glu2200Val
XM_011540044.1:c.6464A>T XP_011538346.1:p.Glu2155Val
XM_011540045.1:c.6599A>T XP_011538347.1:p.Glu2200Val
XM_011540046.1:c.6059A>T XP_011538348.1:p.Glu2020Val
XM_011540047.1:c.5417A>T XP_011538349.1:p.Glu1806Val
XM_011540048.1:c.6599A>T XP_011538350.1:p.Glu2200Val
XM_011540049.1:c.6599A>T XP_011538351.1:p.Glu2200Val
XM_011540050.1:c.6599A>T XP_011538352.1:p.Glu2200Val
XM_011540051.1:c.6599A>T XP_011538353.1:p.Glu2200Val
XM_011540052.1:c.2927A>T XP_011538354.1:p.Glu976Val
XR_945796.1:n.6842A>T
NM_022124.6:c.6404A>T MANE Select NP_071407.4:p.Glu2135Val