Canonical Allele Identifier: CA377154933
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71793346T>A , CM000672.2:g.71793346T>A GRCh38
NC_000010.10:g.73553103T>A , CM000672.1:g.73553103T>A GRCh37
NC_000010.9:g.73223109T>A NCBI36
NG_008835.1:g.401400T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.6418T>A MANE Select ENSP00000224721.9:p.Tyr2140Asn
ENST00000224721.10:c.6433T>A ENSP00000224721.8:p.Tyr2145Asn
ENST00000622827.4:c.6418T>A ENSP00000483211.1:p.Tyr2140Asn
NM_022124.5:c.6418T>A NP_071407.4:p.Tyr2140Asn
XM_006717940.2:c.6613T>A XP_006718003.1:p.Tyr2205Asn
XM_006717942.2:c.6547T>A XP_006718005.1:p.Tyr2183Asn
XM_011540039.1:c.6610T>A XP_011538341.1:p.Tyr2204Asn
XM_011540040.1:c.6607T>A XP_011538342.1:p.Tyr2203Asn
XM_011540041.1:c.6553T>A XP_011538343.1:p.Tyr2185Asn
XM_011540042.1:c.6577+36T>A XP_011538344.1:n.6577+36T>A
XM_011540043.1:c.6613T>A XP_011538345.1:p.Tyr2205Asn
XM_011540044.1:c.6478T>A XP_011538346.1:p.Tyr2160Asn
XM_011540045.1:c.6613T>A XP_011538347.1:p.Tyr2205Asn
XM_011540046.1:c.6073T>A XP_011538348.1:p.Tyr2025Asn
XM_011540047.1:c.5431T>A XP_011538349.1:p.Tyr1811Asn
XM_011540048.1:c.6613T>A XP_011538350.1:p.Tyr2205Asn
XM_011540049.1:c.6613T>A XP_011538351.1:p.Tyr2205Asn
XM_011540050.1:c.6613T>A XP_011538352.1:p.Tyr2205Asn
XM_011540051.1:c.6613T>A XP_011538353.1:p.Tyr2205Asn
XM_011540052.1:c.2941T>A XP_011538354.1:p.Tyr981Asn
XR_945796.1:n.6856T>A
NM_022124.6:c.6418T>A MANE Select NP_071407.4:p.Tyr2140Asn