Canonical Allele Identifier: CA377131332
Gene: CDH23 HGNC NCBI

Linked Data

gnomAD v4: 10-71807537-T-C
MyVariant Identifiers: chr10:g.73567294T>C (hg19) chr10:g.71807537T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71807537T>C , CM000672.2:g.71807537T>C GRCh38
NC_000010.10:g.73567294T>C , CM000672.1:g.73567294T>C GRCh37
NC_000010.9:g.73237300T>C NCBI36
NG_008835.1:g.415591T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.8330T>C MANE Select ENSP00000224721.9:p.Phe2777Ser
ENST00000642965.1:c.2263T>C ENSP00000495222.1:n.2263T>C
ENST00000647092.1:c.1927T>C ENSP00000495176.1:n.1927T>C
ENST00000224721.10:c.8345T>C ENSP00000224721.8:p.Phe2782Ser
ENST00000398788.4:c.1610T>C ENSP00000381768.3:p.Phe537Ser
ENST00000475158.1:n.1866T>C
ENST00000619887.4:c.1610T>C ENSP00000478374.1:p.Phe537Ser
ENST00000622827.4:c.8330T>C ENSP00000483211.1:p.Phe2777Ser
NM_001171933.1:c.1610T>C NP_001165404.1:p.Phe537Ser
NM_001171934.1:c.1610T>C NP_001165405.1:p.Phe537Ser
NM_022124.5:c.8330T>C NP_071407.4:p.Phe2777Ser
XM_006717940.2:c.8525T>C XP_006718003.1:p.Phe2842Ser
XM_006717942.2:c.8459T>C XP_006718005.1:p.Phe2820Ser
XM_011540039.1:c.8522T>C XP_011538341.1:p.Phe2841Ser
XM_011540040.1:c.8519T>C XP_011538342.1:p.Phe2840Ser
XM_011540041.1:c.8465T>C XP_011538343.1:p.Phe2822Ser
XM_011540042.1:c.8435T>C XP_011538344.1:p.Phe2812Ser
XM_011540043.1:c.8525T>C XP_011538345.1:p.Phe2842Ser
XM_011540044.1:c.8390T>C XP_011538346.1:p.Phe2797Ser
XM_011540045.1:c.8525T>C XP_011538347.1:p.Phe2842Ser
XM_011540046.1:c.7985T>C XP_011538348.1:p.Phe2662Ser
XM_011540047.1:c.7343T>C XP_011538349.1:p.Phe2448Ser
XM_011540052.1:c.4853T>C XP_011538354.1:p.Phe1618Ser
NM_022124.6:c.8330T>C MANE Select NP_071407.4:p.Phe2777Ser
Search 100 bp 5'
Search 100 bp 3'