Canonical Allele Identifier: CA470062253
Gene: CDH23 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.73560419G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71800662G>C , CM000672.2:g.71800662G>C GRCh38
NC_000010.10:g.73560419G>C , CM000672.1:g.73560419G>C GRCh37
NC_000010.9:g.73230425G>C NCBI36
NG_008835.1:g.408716G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.7389G>C MANE Select ENSP00000224721.9:p.Leu2463=
ENST00000642965.1:c.1322G>C ENSP00000495222.1:n.1322G>C
ENST00000647092.1:c.986G>C ENSP00000495176.1:n.986G>C
ENST00000224721.10:c.7404G>C ENSP00000224721.8:p.Leu2468=
ENST00000398788.4:c.669G>C ENSP00000381768.3:p.Leu223=
ENST00000475158.1:n.925G>C
ENST00000619887.4:c.669G>C ENSP00000478374.1:p.Leu223=
ENST00000622827.4:c.7389G>C ENSP00000483211.1:p.Leu2463=
NM_001171933.1:c.669G>C NP_001165404.1:p.Leu223=
NM_001171934.1:c.669G>C NP_001165405.1:p.Leu223=
NM_022124.5:c.7389G>C NP_071407.4:p.Leu2463=
XM_006717940.2:c.7584G>C XP_006718003.1:p.Leu2528=
XM_006717942.2:c.7518G>C XP_006718005.1:p.Leu2506=
XM_011540039.1:c.7581G>C XP_011538341.1:p.Leu2527=
XM_011540040.1:c.7578G>C XP_011538342.1:p.Leu2526=
XM_011540041.1:c.7524G>C XP_011538343.1:p.Leu2508=
XM_011540042.1:c.7494G>C XP_011538344.1:p.Leu2498=
XM_011540043.1:c.7584G>C XP_011538345.1:p.Leu2528=
XM_011540044.1:c.7449G>C XP_011538346.1:p.Leu2483=
XM_011540045.1:c.7584G>C XP_011538347.1:p.Leu2528=
XM_011540046.1:c.7044G>C XP_011538348.1:p.Leu2348=
XM_011540047.1:c.6402G>C XP_011538349.1:p.Leu2134=
XM_011540052.1:c.3912G>C XP_011538354.1:p.Leu1304=
NM_022124.6:c.7389G>C MANE Select NP_071407.4:p.Leu2463=