Canonical Allele Identifier: CA377154939
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71793347A>C , CM000672.2:g.71793347A>C GRCh38
NC_000010.10:g.73553104A>C , CM000672.1:g.73553104A>C GRCh37
NC_000010.9:g.73223110A>C NCBI36
NG_008835.1:g.401401A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.6419A>C MANE Select ENSP00000224721.9:p.Tyr2140Ser
ENST00000224721.10:c.6434A>C ENSP00000224721.8:p.Tyr2145Ser
ENST00000622827.4:c.6419A>C ENSP00000483211.1:p.Tyr2140Ser
NM_022124.5:c.6419A>C NP_071407.4:p.Tyr2140Ser
XM_006717940.2:c.6614A>C XP_006718003.1:p.Tyr2205Ser
XM_006717942.2:c.6548A>C XP_006718005.1:p.Tyr2183Ser
XM_011540039.1:c.6611A>C XP_011538341.1:p.Tyr2204Ser
XM_011540040.1:c.6608A>C XP_011538342.1:p.Tyr2203Ser
XM_011540041.1:c.6554A>C XP_011538343.1:p.Tyr2185Ser
XM_011540042.1:c.6577+37A>C XP_011538344.1:n.6577+37A>C
XM_011540043.1:c.6614A>C XP_011538345.1:p.Tyr2205Ser
XM_011540044.1:c.6479A>C XP_011538346.1:p.Tyr2160Ser
XM_011540045.1:c.6614A>C XP_011538347.1:p.Tyr2205Ser
XM_011540046.1:c.6074A>C XP_011538348.1:p.Tyr2025Ser
XM_011540047.1:c.5432A>C XP_011538349.1:p.Tyr1811Ser
XM_011540048.1:c.6614A>C XP_011538350.1:p.Tyr2205Ser
XM_011540049.1:c.6614A>C XP_011538351.1:p.Tyr2205Ser
XM_011540050.1:c.6614A>C XP_011538352.1:p.Tyr2205Ser
XM_011540051.1:c.6614A>C XP_011538353.1:p.Tyr2205Ser
XM_011540052.1:c.2942A>C XP_011538354.1:p.Tyr981Ser
XR_945796.1:n.6857A>C
NM_022124.6:c.6419A>C MANE Select NP_071407.4:p.Tyr2140Ser