Canonical Allele Identifier: CA377162314
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71806186G>C , CM000672.2:g.71806186G>C GRCh38
NC_000010.10:g.73565943G>C , CM000672.1:g.73565943G>C GRCh37
NC_000010.9:g.73235949G>C NCBI36
NG_008835.1:g.414240G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.8083G>C MANE Select ENSP00000224721.9:p.Asp2695His
ENST00000642965.1:c.2016G>C ENSP00000495222.1:n.2016G>C
ENST00000647092.1:c.1680G>C ENSP00000495176.1:n.1680G>C
ENST00000224721.10:c.8098G>C ENSP00000224721.8:p.Asp2700His
ENST00000398788.4:c.1363G>C ENSP00000381768.3:p.Asp455His
ENST00000475158.1:n.1619G>C
ENST00000619887.4:c.1363G>C ENSP00000478374.1:p.Asp455His
ENST00000622827.4:c.8083G>C ENSP00000483211.1:p.Asp2695His
NM_001171933.1:c.1363G>C NP_001165404.1:p.Asp455His
NM_001171934.1:c.1363G>C NP_001165405.1:p.Asp455His
NM_022124.5:c.8083G>C NP_071407.4:p.Asp2695His
XM_006717940.2:c.8278G>C XP_006718003.1:p.Asp2760His
XM_006717942.2:c.8212G>C XP_006718005.1:p.Asp2738His
XM_011540039.1:c.8275G>C XP_011538341.1:p.Asp2759His
XM_011540040.1:c.8272G>C XP_011538342.1:p.Asp2758His
XM_011540041.1:c.8218G>C XP_011538343.1:p.Asp2740His
XM_011540042.1:c.8188G>C XP_011538344.1:p.Asp2730His
XM_011540043.1:c.8278G>C XP_011538345.1:p.Asp2760His
XM_011540044.1:c.8143G>C XP_011538346.1:p.Asp2715His
XM_011540045.1:c.8278G>C XP_011538347.1:p.Asp2760His
XM_011540046.1:c.7738G>C XP_011538348.1:p.Asp2580His
XM_011540047.1:c.7096G>C XP_011538349.1:p.Asp2366His
XM_011540052.1:c.4606G>C XP_011538354.1:p.Asp1536His
NM_022124.6:c.8083G>C MANE Select NP_071407.4:p.Asp2695His