Canonical Allele Identifier: CA377158183

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73558269C>G (hg19) ; chr10:g.71798512C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798512C>G , CM000672.2:g.71798512C>G	GRCh38
NC_000010.10:g.73558269C>G , CM000672.1:g.73558269C>G	GRCh37
NC_000010.9:g.73228275C>G	NCBI36
NG_008835.1:g.406566C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6988C>G MANE Select	ENSP00000224721.9:p.Leu2330Val
ENST00000642965.1:c.921C>G	ENSP00000495222.1:n.921C>G
ENST00000647092.1:c.585C>G	ENSP00000495176.1:n.585C>G
ENST00000224721.10:c.7003C>G	ENSP00000224721.8:p.Leu2335Val
ENST00000398788.4:c.268C>G	ENSP00000381768.3:p.Leu90Val
ENST00000475158.1:n.524C>G
ENST00000619887.4:c.268C>G	ENSP00000478374.1:p.Leu90Val
ENST00000622827.4:c.6988C>G	ENSP00000483211.1:p.Leu2330Val
NM_001171933.1:c.268C>G	NP_001165404.1:p.Leu90Val
NM_001171934.1:c.268C>G	NP_001165405.1:p.Leu90Val
NM_022124.5:c.6988C>G	NP_071407.4:p.Leu2330Val
XM_006717940.2:c.7183C>G	XP_006718003.1:p.Leu2395Val
XM_006717942.2:c.7117C>G	XP_006718005.1:p.Leu2373Val
XM_011540039.1:c.7180C>G	XP_011538341.1:p.Leu2394Val
XM_011540040.1:c.7177C>G	XP_011538342.1:p.Leu2393Val
XM_011540041.1:c.7123C>G	XP_011538343.1:p.Leu2375Val
XM_011540042.1:c.7093C>G	XP_011538344.1:p.Leu2365Val
XM_011540043.1:c.7183C>G	XP_011538345.1:p.Leu2395Val
XM_011540044.1:c.7048C>G	XP_011538346.1:p.Leu2350Val
XM_011540045.1:c.7183C>G	XP_011538347.1:p.Leu2395Val
XM_011540046.1:c.6643C>G	XP_011538348.1:p.Leu2215Val
XM_011540047.1:c.6001C>G	XP_011538349.1:p.Leu2001Val
XM_011540052.1:c.3511C>G	XP_011538354.1:p.Leu1171Val
NM_022124.6:c.6988C>G MANE Select	NP_071407.4:p.Leu2330Val