Canonical Allele Identifier: CA377157876
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71798429T>A , CM000672.2:g.71798429T>A GRCh38
NC_000010.10:g.73558186T>A , CM000672.1:g.73558186T>A GRCh37
NC_000010.9:g.73228192T>A NCBI36
NG_008835.1:g.406483T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.6905T>A MANE Select ENSP00000224721.9:p.Met2302Lys
ENST00000642965.1:c.838T>A ENSP00000495222.1:n.838T>A
ENST00000647092.1:c.502T>A ENSP00000495176.1:n.502T>A
ENST00000224721.10:c.6920T>A ENSP00000224721.8:p.Met2307Lys
ENST00000398788.4:c.185T>A ENSP00000381768.3:p.Met62Lys
ENST00000475158.1:n.441T>A
ENST00000619887.4:c.185T>A ENSP00000478374.1:p.Met62Lys
ENST00000622827.4:c.6905T>A ENSP00000483211.1:p.Met2302Lys
NM_001171933.1:c.185T>A NP_001165404.1:p.Met62Lys
NM_001171934.1:c.185T>A NP_001165405.1:p.Met62Lys
NM_022124.5:c.6905T>A NP_071407.4:p.Met2302Lys
XM_006717940.2:c.7100T>A XP_006718003.1:p.Met2367Lys
XM_006717942.2:c.7034T>A XP_006718005.1:p.Met2345Lys
XM_011540039.1:c.7097T>A XP_011538341.1:p.Met2366Lys
XM_011540040.1:c.7094T>A XP_011538342.1:p.Met2365Lys
XM_011540041.1:c.7040T>A XP_011538343.1:p.Met2347Lys
XM_011540042.1:c.7010T>A XP_011538344.1:p.Met2337Lys
XM_011540043.1:c.7100T>A XP_011538345.1:p.Met2367Lys
XM_011540044.1:c.6965T>A XP_011538346.1:p.Met2322Lys
XM_011540045.1:c.7100T>A XP_011538347.1:p.Met2367Lys
XM_011540046.1:c.6560T>A XP_011538348.1:p.Met2187Lys
XM_011540047.1:c.5918T>A XP_011538349.1:p.Met1973Lys
XM_011540052.1:c.3428T>A XP_011538354.1:p.Met1143Lys
NM_022124.6:c.6905T>A MANE Select NP_071407.4:p.Met2302Lys