Canonical Allele Identifier: CA377131361

Gene: CDH23

Linked Data

• dbSNP Id: rs1301559791
• MyVariant Identifiers: chr10:g.73567306C>G (hg19) ; chr10:g.71807549C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71807549C>G , CM000672.2:g.71807549C>G	GRCh38
NC_000010.10:g.73567306C>G , CM000672.1:g.73567306C>G	GRCh37
NC_000010.9:g.73237312C>G	NCBI36
NG_008835.1:g.415603C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.8342C>G MANE Select	ENSP00000224721.9:p.Pro2781Arg
ENST00000642965.1:c.2275C>G	ENSP00000495222.1:n.2275C>G
ENST00000647092.1:c.1939C>G	ENSP00000495176.1:n.1939C>G
ENST00000224721.10:c.8357C>G	ENSP00000224721.8:p.Pro2786Arg
ENST00000398788.4:c.1622C>G	ENSP00000381768.3:p.Pro541Arg
ENST00000475158.1:n.1878C>G
ENST00000619887.4:c.1622C>G	ENSP00000478374.1:p.Pro541Arg
ENST00000622827.4:c.8342C>G	ENSP00000483211.1:p.Pro2781Arg
NM_001171933.1:c.1622C>G	NP_001165404.1:p.Pro541Arg
NM_001171934.1:c.1622C>G	NP_001165405.1:p.Pro541Arg
NM_022124.5:c.8342C>G	NP_071407.4:p.Pro2781Arg
XM_006717940.2:c.8537C>G	XP_006718003.1:p.Pro2846Arg
XM_006717942.2:c.8471C>G	XP_006718005.1:p.Pro2824Arg
XM_011540039.1:c.8534C>G	XP_011538341.1:p.Pro2845Arg
XM_011540040.1:c.8531C>G	XP_011538342.1:p.Pro2844Arg
XM_011540041.1:c.8477C>G	XP_011538343.1:p.Pro2826Arg
XM_011540042.1:c.8447C>G	XP_011538344.1:p.Pro2816Arg
XM_011540043.1:c.8537C>G	XP_011538345.1:p.Pro2846Arg
XM_011540044.1:c.8402C>G	XP_011538346.1:p.Pro2801Arg
XM_011540045.1:c.8537C>G	XP_011538347.1:p.Pro2846Arg
XM_011540046.1:c.7997C>G	XP_011538348.1:p.Pro2666Arg
XM_011540047.1:c.7355C>G	XP_011538349.1:p.Pro2452Arg
XM_011540052.1:c.4865C>G	XP_011538354.1:p.Pro1622Arg
NM_022124.6:c.8342C>G MANE Select	NP_071407.4:p.Pro2781Arg