Canonical Allele Identifier: CA377160699
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71740920C>G , CM000672.2:g.71740920C>G GRCh38
NC_000010.10:g.73500677C>G , CM000672.1:g.73500677C>G GRCh37
NC_000010.9:g.73170683C>G NCBI36
NG_008835.1:g.348974C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.4587C>G MANE Select ENSP00000224721.9:p.Ser1529Arg
ENST00000224721.10:c.4602C>G ENSP00000224721.8:p.Ser1534Arg
ENST00000398792.3:n.1276C>G
ENST00000622827.4:c.4587C>G ENSP00000483211.1:p.Ser1529Arg
NM_022124.5:c.4587C>G NP_071407.4:p.Ser1529Arg
XM_006717940.2:c.4782C>G XP_006718003.1:p.Ser1594Arg
XM_006717942.2:c.4716C>G XP_006718005.1:p.Ser1572Arg
XM_011540039.1:c.4779C>G XP_011538341.1:p.Ser1593Arg
XM_011540040.1:c.4776C>G XP_011538342.1:p.Ser1592Arg
XM_011540041.1:c.4722C>G XP_011538343.1:p.Ser1574Arg
XM_011540042.1:c.4782C>G XP_011538344.1:p.Ser1594Arg
XM_011540043.1:c.4782C>G XP_011538345.1:p.Ser1594Arg
XM_011540044.1:c.4647C>G XP_011538346.1:p.Ser1549Arg
XM_011540045.1:c.4782C>G XP_011538347.1:p.Ser1594Arg
XM_011540046.1:c.4242C>G XP_011538348.1:p.Ser1414Arg
XM_011540047.1:c.3600C>G XP_011538349.1:p.Ser1200Arg
XM_011540048.1:c.4782C>G XP_011538350.1:p.Ser1594Arg
XM_011540049.1:c.4782C>G XP_011538351.1:p.Ser1594Arg
XM_011540050.1:c.4782C>G XP_011538352.1:p.Ser1594Arg
XM_011540051.1:c.4782C>G XP_011538353.1:p.Ser1594Arg
XM_011540052.1:c.1110C>G XP_011538354.1:p.Ser370Arg
XM_011540053.1:c.4782C>G XP_011538355.1:p.Ser1594Arg
XR_945796.1:n.5025C>G
NM_022124.6:c.4587C>G MANE Select NP_071407.4:p.Ser1529Arg