Canonical Allele Identifier: CA377158283

Gene: CDH23

Linked Data

• gnomAD v4: 10-71798530-C-G
• MyVariant Identifiers: chr10:g.73558287C>G (hg19) ; chr10:g.71798530C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798530C>G , CM000672.2:g.71798530C>G	GRCh38
NC_000010.10:g.73558287C>G , CM000672.1:g.73558287C>G	GRCh37
NC_000010.9:g.73228293C>G	NCBI36
NG_008835.1:g.406584C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7006C>G MANE Select	ENSP00000224721.9:p.Leu2336Val
ENST00000642965.1:c.939C>G	ENSP00000495222.1:n.939C>G
ENST00000647092.1:c.603C>G	ENSP00000495176.1:n.603C>G
ENST00000224721.10:c.7021C>G	ENSP00000224721.8:p.Leu2341Val
ENST00000398788.4:c.286C>G	ENSP00000381768.3:p.Leu96Val
ENST00000475158.1:n.542C>G
ENST00000619887.4:c.286C>G	ENSP00000478374.1:p.Leu96Val
ENST00000622827.4:c.7006C>G	ENSP00000483211.1:p.Leu2336Val
NM_001171933.1:c.286C>G	NP_001165404.1:p.Leu96Val
NM_001171934.1:c.286C>G	NP_001165405.1:p.Leu96Val
NM_022124.5:c.7006C>G	NP_071407.4:p.Leu2336Val
XM_006717940.2:c.7201C>G	XP_006718003.1:p.Leu2401Val
XM_006717942.2:c.7135C>G	XP_006718005.1:p.Leu2379Val
XM_011540039.1:c.7198C>G	XP_011538341.1:p.Leu2400Val
XM_011540040.1:c.7195C>G	XP_011538342.1:p.Leu2399Val
XM_011540041.1:c.7141C>G	XP_011538343.1:p.Leu2381Val
XM_011540042.1:c.7111C>G	XP_011538344.1:p.Leu2371Val
XM_011540043.1:c.7201C>G	XP_011538345.1:p.Leu2401Val
XM_011540044.1:c.7066C>G	XP_011538346.1:p.Leu2356Val
XM_011540045.1:c.7201C>G	XP_011538347.1:p.Leu2401Val
XM_011540046.1:c.6661C>G	XP_011538348.1:p.Leu2221Val
XM_011540047.1:c.6019C>G	XP_011538349.1:p.Leu2007Val
XM_011540052.1:c.3529C>G	XP_011538354.1:p.Leu1177Val
NM_022124.6:c.7006C>G MANE Select	NP_071407.4:p.Leu2336Val