Canonical Allele Identifier: CA377131669

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73567467G>C (hg19) ; chr10:g.71807710G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71807710G>C , CM000672.2:g.71807710G>C	GRCh38
NC_000010.10:g.73567467G>C , CM000672.1:g.73567467G>C	GRCh37
NC_000010.9:g.73237473G>C	NCBI36
NG_008835.1:g.415764G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.8503G>C MANE Select	ENSP00000224721.9:p.Val2835Leu
ENST00000642965.1:c.2436G>C	ENSP00000495222.1:n.2436G>C
ENST00000647092.1:c.2100G>C	ENSP00000495176.1:n.2100G>C
ENST00000224721.10:c.8518G>C	ENSP00000224721.8:p.Val2840Leu
ENST00000398788.4:c.1783G>C	ENSP00000381768.3:p.Val595Leu
ENST00000475158.1:n.2039G>C
ENST00000619887.4:c.1783G>C	ENSP00000478374.1:p.Val595Leu
ENST00000622827.4:c.8503G>C	ENSP00000483211.1:p.Val2835Leu
NM_001171933.1:c.1783G>C	NP_001165404.1:p.Val595Leu
NM_001171934.1:c.1783G>C	NP_001165405.1:p.Val595Leu
NM_022124.5:c.8503G>C	NP_071407.4:p.Val2835Leu
XM_006717940.2:c.8698G>C	XP_006718003.1:p.Val2900Leu
XM_006717942.2:c.8632G>C	XP_006718005.1:p.Val2878Leu
XM_011540039.1:c.8695G>C	XP_011538341.1:p.Val2899Leu
XM_011540040.1:c.8692G>C	XP_011538342.1:p.Val2898Leu
XM_011540041.1:c.8638G>C	XP_011538343.1:p.Val2880Leu
XM_011540042.1:c.8608G>C	XP_011538344.1:p.Val2870Leu
XM_011540043.1:c.8698G>C	XP_011538345.1:p.Val2900Leu
XM_011540044.1:c.8563G>C	XP_011538346.1:p.Val2855Leu
XM_011540045.1:c.8698G>C	XP_011538347.1:p.Val2900Leu
XM_011540046.1:c.8158G>C	XP_011538348.1:p.Val2720Leu
XM_011540047.1:c.7516G>C	XP_011538349.1:p.Val2506Leu
XM_011540052.1:c.5026G>C	XP_011538354.1:p.Val1676Leu
NM_022124.6:c.8503G>C MANE Select	NP_071407.4:p.Val2835Leu