Canonical Allele Identifier: CA377157754

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73558152C>G (hg19) ; chr10:g.71798395C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798395C>G , CM000672.2:g.71798395C>G	GRCh38
NC_000010.10:g.73558152C>G , CM000672.1:g.73558152C>G	GRCh37
NC_000010.9:g.73228158C>G	NCBI36
NG_008835.1:g.406449C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6871C>G MANE Select	ENSP00000224721.9:p.Pro2291Ala
ENST00000642965.1:c.804C>G	ENSP00000495222.1:n.804C>G
ENST00000647092.1:c.468C>G	ENSP00000495176.1:n.468C>G
ENST00000224721.10:c.6886C>G	ENSP00000224721.8:p.Pro2296Ala
ENST00000398788.4:c.151C>G	ENSP00000381768.3:p.Pro51Ala
ENST00000475158.1:n.407C>G
ENST00000619887.4:c.151C>G	ENSP00000478374.1:p.Pro51Ala
ENST00000622827.4:c.6871C>G	ENSP00000483211.1:p.Pro2291Ala
NM_001171933.1:c.151C>G	NP_001165404.1:p.Pro51Ala
NM_001171934.1:c.151C>G	NP_001165405.1:p.Pro51Ala
NM_022124.5:c.6871C>G	NP_071407.4:p.Pro2291Ala
XM_006717940.2:c.7066C>G	XP_006718003.1:p.Pro2356Ala
XM_006717942.2:c.7000C>G	XP_006718005.1:p.Pro2334Ala
XM_011540039.1:c.7063C>G	XP_011538341.1:p.Pro2355Ala
XM_011540040.1:c.7060C>G	XP_011538342.1:p.Pro2354Ala
XM_011540041.1:c.7006C>G	XP_011538343.1:p.Pro2336Ala
XM_011540042.1:c.6976C>G	XP_011538344.1:p.Pro2326Ala
XM_011540043.1:c.7066C>G	XP_011538345.1:p.Pro2356Ala
XM_011540044.1:c.6931C>G	XP_011538346.1:p.Pro2311Ala
XM_011540045.1:c.7066C>G	XP_011538347.1:p.Pro2356Ala
XM_011540046.1:c.6526C>G	XP_011538348.1:p.Pro2176Ala
XM_011540047.1:c.5884C>G	XP_011538349.1:p.Pro1962Ala
XM_011540052.1:c.3394C>G	XP_011538354.1:p.Pro1132Ala
NM_022124.6:c.6871C>G MANE Select	NP_071407.4:p.Pro2291Ala