Canonical Allele Identifier: CA5546060
Gene: CDH23 HGNC NCBI

Linked Data

dbSNP Id: rs375329233

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.6343C>G MANE Select ENSP00000224721.9:p.Arg2115Gly
ENST00000224721.10:c.6358C>G ENSP00000224721.8:p.Arg2120Gly
ENST00000622827.4:c.6343C>G ENSP00000483211.1:p.Arg2115Gly
NM_022124.5:c.6343C>G NP_071407.4:p.Arg2115Gly
XM_006717940.2:c.6538C>G XP_006718003.1:p.Arg2180Gly
XM_006717942.2:c.6472C>G XP_006718005.1:p.Arg2158Gly
XM_011540039.1:c.6535C>G XP_011538341.1:p.Arg2179Gly
XM_011540040.1:c.6532C>G XP_011538342.1:p.Arg2178Gly
XM_011540041.1:c.6478C>G XP_011538343.1:p.Arg2160Gly
XM_011540042.1:c.6538C>G XP_011538344.1:p.Arg2180Gly
XM_011540043.1:c.6538C>G XP_011538345.1:p.Arg2180Gly
XM_011540044.1:c.6403C>G XP_011538346.1:p.Arg2135Gly
XM_011540045.1:c.6538C>G XP_011538347.1:p.Arg2180Gly
XM_011540046.1:c.5998C>G XP_011538348.1:p.Arg2000Gly
XM_011540047.1:c.5356C>G XP_011538349.1:p.Arg1786Gly
XM_011540048.1:c.6538C>G XP_011538350.1:p.Arg2180Gly
XM_011540049.1:c.6538C>G XP_011538351.1:p.Arg2180Gly
XM_011540050.1:c.6538C>G XP_011538352.1:p.Arg2180Gly
XM_011540051.1:c.6538C>G XP_011538353.1:p.Arg2180Gly
XM_011540052.1:c.2866C>G XP_011538354.1:p.Arg956Gly
XR_945796.1:n.6781C>G
NM_022124.6:c.6343C>G MANE Select NP_071407.4:p.Arg2115Gly