Canonical Allele Identifier: CA377131500
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71807624C>A , CM000672.2:g.71807624C>A GRCh38
NC_000010.10:g.73567381C>A , CM000672.1:g.73567381C>A GRCh37
NC_000010.9:g.73237387C>A NCBI36
NG_008835.1:g.415678C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.8417C>A MANE Select ENSP00000224721.9:p.Ser2806Tyr
ENST00000642965.1:c.2350C>A ENSP00000495222.1:n.2350C>A
ENST00000647092.1:c.2014C>A ENSP00000495176.1:n.2014C>A
ENST00000224721.10:c.8432C>A ENSP00000224721.8:p.Ser2811Tyr
ENST00000398788.4:c.1697C>A ENSP00000381768.3:p.Ser566Tyr
ENST00000475158.1:n.1953C>A
ENST00000619887.4:c.1697C>A ENSP00000478374.1:p.Ser566Tyr
ENST00000622827.4:c.8417C>A ENSP00000483211.1:p.Ser2806Tyr
NM_001171933.1:c.1697C>A NP_001165404.1:p.Ser566Tyr
NM_001171934.1:c.1697C>A NP_001165405.1:p.Ser566Tyr
NM_022124.5:c.8417C>A NP_071407.4:p.Ser2806Tyr
XM_006717940.2:c.8612C>A XP_006718003.1:p.Ser2871Tyr
XM_006717942.2:c.8546C>A XP_006718005.1:p.Ser2849Tyr
XM_011540039.1:c.8609C>A XP_011538341.1:p.Ser2870Tyr
XM_011540040.1:c.8606C>A XP_011538342.1:p.Ser2869Tyr
XM_011540041.1:c.8552C>A XP_011538343.1:p.Ser2851Tyr
XM_011540042.1:c.8522C>A XP_011538344.1:p.Ser2841Tyr
XM_011540043.1:c.8612C>A XP_011538345.1:p.Ser2871Tyr
XM_011540044.1:c.8477C>A XP_011538346.1:p.Ser2826Tyr
XM_011540045.1:c.8612C>A XP_011538347.1:p.Ser2871Tyr
XM_011540046.1:c.8072C>A XP_011538348.1:p.Ser2691Tyr
XM_011540047.1:c.7430C>A XP_011538349.1:p.Ser2477Tyr
XM_011540052.1:c.4940C>A XP_011538354.1:p.Ser1647Tyr
NM_022124.6:c.8417C>A MANE Select NP_071407.4:p.Ser2806Tyr