Canonical Allele Identifier: CA377158134
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71798504T>C , CM000672.2:g.71798504T>C GRCh38
NC_000010.10:g.73558261T>C , CM000672.1:g.73558261T>C GRCh37
NC_000010.9:g.73228267T>C NCBI36
NG_008835.1:g.406558T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.6980T>C MANE Select ENSP00000224721.9:p.Leu2327Pro
ENST00000642965.1:c.913T>C ENSP00000495222.1:n.913T>C
ENST00000647092.1:c.577T>C ENSP00000495176.1:n.577T>C
ENST00000224721.10:c.6995T>C ENSP00000224721.8:p.Leu2332Pro
ENST00000398788.4:c.260T>C ENSP00000381768.3:p.Leu87Pro
ENST00000475158.1:n.516T>C
ENST00000619887.4:c.260T>C ENSP00000478374.1:p.Leu87Pro
ENST00000622827.4:c.6980T>C ENSP00000483211.1:p.Leu2327Pro
NM_001171933.1:c.260T>C NP_001165404.1:p.Leu87Pro
NM_001171934.1:c.260T>C NP_001165405.1:p.Leu87Pro
NM_022124.5:c.6980T>C NP_071407.4:p.Leu2327Pro
XM_006717940.2:c.7175T>C XP_006718003.1:p.Leu2392Pro
XM_006717942.2:c.7109T>C XP_006718005.1:p.Leu2370Pro
XM_011540039.1:c.7172T>C XP_011538341.1:p.Leu2391Pro
XM_011540040.1:c.7169T>C XP_011538342.1:p.Leu2390Pro
XM_011540041.1:c.7115T>C XP_011538343.1:p.Leu2372Pro
XM_011540042.1:c.7085T>C XP_011538344.1:p.Leu2362Pro
XM_011540043.1:c.7175T>C XP_011538345.1:p.Leu2392Pro
XM_011540044.1:c.7040T>C XP_011538346.1:p.Leu2347Pro
XM_011540045.1:c.7175T>C XP_011538347.1:p.Leu2392Pro
XM_011540046.1:c.6635T>C XP_011538348.1:p.Leu2212Pro
XM_011540047.1:c.5993T>C XP_011538349.1:p.Leu1998Pro
XM_011540052.1:c.3503T>C XP_011538354.1:p.Leu1168Pro
NM_022124.6:c.6980T>C MANE Select NP_071407.4:p.Leu2327Pro