Canonical Allele Identifier: CA377154827
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71793331G>T , CM000672.2:g.71793331G>T GRCh38
NC_000010.10:g.73553088G>T , CM000672.1:g.73553088G>T GRCh37
NC_000010.9:g.73223094G>T NCBI36
NG_008835.1:g.401385G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.6403G>T MANE Select ENSP00000224721.9:p.Glu2135Ter
ENST00000224721.10:c.6418G>T ENSP00000224721.8:p.Glu2140Ter
ENST00000622827.4:c.6403G>T ENSP00000483211.1:p.Glu2135Ter
NM_022124.5:c.6403G>T NP_071407.4:p.Glu2135Ter
XM_006717940.2:c.6598G>T XP_006718003.1:p.Glu2200Ter
XM_006717942.2:c.6532G>T XP_006718005.1:p.Glu2178Ter
XM_011540039.1:c.6595G>T XP_011538341.1:p.Glu2199Ter
XM_011540040.1:c.6592G>T XP_011538342.1:p.Glu2198Ter
XM_011540041.1:c.6538G>T XP_011538343.1:p.Glu2180Ter
XM_011540042.1:c.6577+21G>T XP_011538344.1:n.6577+21G>T
XM_011540043.1:c.6598G>T XP_011538345.1:p.Glu2200Ter
XM_011540044.1:c.6463G>T XP_011538346.1:p.Glu2155Ter
XM_011540045.1:c.6598G>T XP_011538347.1:p.Glu2200Ter
XM_011540046.1:c.6058G>T XP_011538348.1:p.Glu2020Ter
XM_011540047.1:c.5416G>T XP_011538349.1:p.Glu1806Ter
XM_011540048.1:c.6598G>T XP_011538350.1:p.Glu2200Ter
XM_011540049.1:c.6598G>T XP_011538351.1:p.Glu2200Ter
XM_011540050.1:c.6598G>T XP_011538352.1:p.Glu2200Ter
XM_011540051.1:c.6598G>T XP_011538353.1:p.Glu2200Ter
XM_011540052.1:c.2926G>T XP_011538354.1:p.Glu976Ter
XR_945796.1:n.6841G>T
NM_022124.6:c.6403G>T MANE Select NP_071407.4:p.Glu2135Ter