Canonical Allele Identifier: CA377158516
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71798572T>A , CM000672.2:g.71798572T>A GRCh38
NC_000010.10:g.73558329T>A , CM000672.1:g.73558329T>A GRCh37
NC_000010.9:g.73228335T>A NCBI36
NG_008835.1:g.406626T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.7048T>A MANE Select ENSP00000224721.9:p.Ser2350Thr
ENST00000642965.1:c.981T>A ENSP00000495222.1:n.981T>A
ENST00000647092.1:c.645T>A ENSP00000495176.1:n.645T>A
ENST00000224721.10:c.7063T>A ENSP00000224721.8:p.Ser2355Thr
ENST00000398788.4:c.328T>A ENSP00000381768.3:p.Ser110Thr
ENST00000475158.1:n.584T>A
ENST00000619887.4:c.328T>A ENSP00000478374.1:p.Ser110Thr
ENST00000622827.4:c.7048T>A ENSP00000483211.1:p.Ser2350Thr
NM_001171933.1:c.328T>A NP_001165404.1:p.Ser110Thr
NM_001171934.1:c.328T>A NP_001165405.1:p.Ser110Thr
NM_022124.5:c.7048T>A NP_071407.4:p.Ser2350Thr
XM_006717940.2:c.7243T>A XP_006718003.1:p.Ser2415Thr
XM_006717942.2:c.7177T>A XP_006718005.1:p.Ser2393Thr
XM_011540039.1:c.7240T>A XP_011538341.1:p.Ser2414Thr
XM_011540040.1:c.7237T>A XP_011538342.1:p.Ser2413Thr
XM_011540041.1:c.7183T>A XP_011538343.1:p.Ser2395Thr
XM_011540042.1:c.7153T>A XP_011538344.1:p.Ser2385Thr
XM_011540043.1:c.7243T>A XP_011538345.1:p.Ser2415Thr
XM_011540044.1:c.7108T>A XP_011538346.1:p.Ser2370Thr
XM_011540045.1:c.7243T>A XP_011538347.1:p.Ser2415Thr
XM_011540046.1:c.6703T>A XP_011538348.1:p.Ser2235Thr
XM_011540047.1:c.6061T>A XP_011538349.1:p.Ser2021Thr
XM_011540052.1:c.3571T>A XP_011538354.1:p.Ser1191Thr
NM_022124.6:c.7048T>A MANE Select NP_071407.4:p.Ser2350Thr