Canonical Allele Identifier: CA377159414
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71799565A>G , CM000672.2:g.71799565A>G GRCh38
NC_000010.10:g.73559322A>G , CM000672.1:g.73559322A>G GRCh37
NC_000010.9:g.73229328A>G NCBI36
NG_008835.1:g.407619A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.7298A>G MANE Select ENSP00000224721.9:p.Asn2433Ser
ENST00000642965.1:c.1231A>G ENSP00000495222.1:n.1231A>G
ENST00000647092.1:c.895A>G ENSP00000495176.1:n.895A>G
ENST00000224721.10:c.7313A>G ENSP00000224721.8:p.Asn2438Ser
ENST00000398788.4:c.578A>G ENSP00000381768.3:p.Asn193Ser
ENST00000475158.1:n.834A>G
ENST00000619887.4:c.578A>G ENSP00000478374.1:p.Asn193Ser
ENST00000622827.4:c.7298A>G ENSP00000483211.1:p.Asn2433Ser
NM_001171933.1:c.578A>G NP_001165404.1:p.Asn193Ser
NM_001171934.1:c.578A>G NP_001165405.1:p.Asn193Ser
NM_022124.5:c.7298A>G NP_071407.4:p.Asn2433Ser
XM_006717940.2:c.7493A>G XP_006718003.1:p.Asn2498Ser
XM_006717942.2:c.7427A>G XP_006718005.1:p.Asn2476Ser
XM_011540039.1:c.7490A>G XP_011538341.1:p.Asn2497Ser
XM_011540040.1:c.7487A>G XP_011538342.1:p.Asn2496Ser
XM_011540041.1:c.7433A>G XP_011538343.1:p.Asn2478Ser
XM_011540042.1:c.7403A>G XP_011538344.1:p.Asn2468Ser
XM_011540043.1:c.7493A>G XP_011538345.1:p.Asn2498Ser
XM_011540044.1:c.7358A>G XP_011538346.1:p.Asn2453Ser
XM_011540045.1:c.7493A>G XP_011538347.1:p.Asn2498Ser
XM_011540046.1:c.6953A>G XP_011538348.1:p.Asn2318Ser
XM_011540047.1:c.6311A>G XP_011538349.1:p.Asn2104Ser
XM_011540052.1:c.3821A>G XP_011538354.1:p.Asn1274Ser
NM_022124.6:c.7298A>G MANE Select NP_071407.4:p.Asn2433Ser