Canonical Allele Identifier: CA377133209
Gene: CDH23 HGNC NCBI

Linked Data

dbSNP Id: rs1864963021
MyVariant Identifiers: chr10:g.73447422C>T (hg19) chr10:g.71687665C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71687665C>T , CM000672.2:g.71687665C>T GRCh38
NC_000010.10:g.73447422C>T , CM000672.1:g.73447422C>T GRCh37
NC_000010.9:g.73117428C>T NCBI36
NG_008835.1:g.295719C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.2005C>T MANE Select ENSP00000224721.9:p.Pro669Ser
ENST00000398809.9:c.2005C>T ENSP00000381789.5:p.Pro669Ser
ENST00000442677.4:c.2005C>T ENSP00000388894.3:p.Pro669Ser
ENST00000466757.8:c.1436C>T
ENST00000224721.10:c.2020C>T ENSP00000224721.8:p.Pro674Ser
ENST00000299366.11:c.2005C>T ENSP00000299366.8:p.Pro669Ser
ENST00000398809.8:c.2005C>T ENSP00000381789.5:p.Pro669Ser
ENST00000442677.3:c.780C>T
ENST00000466757.7:c.1436C>T
ENST00000616684.4:c.2005C>T ENSP00000482036.2:p.Pro669Ser
ENST00000622827.4:c.2005C>T ENSP00000483211.1:p.Pro669Ser
NM_001171930.1:c.2005C>T NP_001165401.1:p.Pro669Ser
NM_001171931.1:c.2005C>T NP_001165402.1:p.Pro669Ser
NM_022124.5:c.2005C>T NP_071407.4:p.Pro669Ser
XM_006717940.2:c.2200C>T XP_006718003.1:p.Pro734Ser
XM_006717942.2:c.2134C>T XP_006718005.1:p.Pro712Ser
XM_011540039.1:c.2200C>T XP_011538341.1:p.Pro734Ser
XM_011540040.1:c.2194C>T XP_011538342.1:p.Pro732Ser
XM_011540041.1:c.2140C>T XP_011538343.1:p.Pro714Ser
XM_011540042.1:c.2200C>T XP_011538344.1:p.Pro734Ser
XM_011540043.1:c.2200C>T XP_011538345.1:p.Pro734Ser
XM_011540044.1:c.2065C>T XP_011538346.1:p.Pro689Ser
XM_011540045.1:c.2200C>T XP_011538347.1:p.Pro734Ser
XM_011540046.1:c.1660C>T XP_011538348.1:p.Pro554Ser
XM_011540047.1:c.1018C>T XP_011538349.1:p.Pro340Ser
XM_011540048.1:c.2200C>T XP_011538350.1:p.Pro734Ser
XM_011540049.1:c.2200C>T XP_011538351.1:p.Pro734Ser
XM_011540050.1:c.2200C>T XP_011538352.1:p.Pro734Ser
XM_011540051.1:c.2200C>T XP_011538353.1:p.Pro734Ser
XM_011540053.1:c.2200C>T XP_011538355.1:p.Pro734Ser
XM_011540054.1:c.2140C>T XP_011538356.1:p.Pro714Ser
XR_945796.1:n.2443C>T
NM_001171930.2:c.2005C>T NP_001165401.1:p.Pro669Ser
NM_001171931.2:c.2005C>T NP_001165402.1:p.Pro669Ser
NM_022124.6:c.2005C>T MANE Select NP_071407.4:p.Pro669Ser
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