Canonical Allele Identifier: CA377157759

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73558153C>G (hg19) ; chr10:g.71798396C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798396C>G , CM000672.2:g.71798396C>G	GRCh38
NC_000010.10:g.73558153C>G , CM000672.1:g.73558153C>G	GRCh37
NC_000010.9:g.73228159C>G	NCBI36
NG_008835.1:g.406450C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6872C>G MANE Select	ENSP00000224721.9:p.Pro2291Arg
ENST00000642965.1:c.805C>G	ENSP00000495222.1:n.805C>G
ENST00000647092.1:c.469C>G	ENSP00000495176.1:n.469C>G
ENST00000224721.10:c.6887C>G	ENSP00000224721.8:p.Pro2296Arg
ENST00000398788.4:c.152C>G	ENSP00000381768.3:p.Pro51Arg
ENST00000475158.1:n.408C>G
ENST00000619887.4:c.152C>G	ENSP00000478374.1:p.Pro51Arg
ENST00000622827.4:c.6872C>G	ENSP00000483211.1:p.Pro2291Arg
NM_001171933.1:c.152C>G	NP_001165404.1:p.Pro51Arg
NM_001171934.1:c.152C>G	NP_001165405.1:p.Pro51Arg
NM_022124.5:c.6872C>G	NP_071407.4:p.Pro2291Arg
XM_006717940.2:c.7067C>G	XP_006718003.1:p.Pro2356Arg
XM_006717942.2:c.7001C>G	XP_006718005.1:p.Pro2334Arg
XM_011540039.1:c.7064C>G	XP_011538341.1:p.Pro2355Arg
XM_011540040.1:c.7061C>G	XP_011538342.1:p.Pro2354Arg
XM_011540041.1:c.7007C>G	XP_011538343.1:p.Pro2336Arg
XM_011540042.1:c.6977C>G	XP_011538344.1:p.Pro2326Arg
XM_011540043.1:c.7067C>G	XP_011538345.1:p.Pro2356Arg
XM_011540044.1:c.6932C>G	XP_011538346.1:p.Pro2311Arg
XM_011540045.1:c.7067C>G	XP_011538347.1:p.Pro2356Arg
XM_011540046.1:c.6527C>G	XP_011538348.1:p.Pro2176Arg
XM_011540047.1:c.5885C>G	XP_011538349.1:p.Pro1962Arg
XM_011540052.1:c.3395C>G	XP_011538354.1:p.Pro1132Arg
NM_022124.6:c.6872C>G MANE Select	NP_071407.4:p.Pro2291Arg