Canonical Allele Identifier: CA377157753

Gene: CDH23

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6871C>A MANE Select	ENSP00000224721.9:p.Pro2291Thr
ENST00000642965.1:c.804C>A	ENSP00000495222.1:n.804C>A
ENST00000647092.1:c.468C>A	ENSP00000495176.1:n.468C>A
ENST00000224721.10:c.6886C>A	ENSP00000224721.8:p.Pro2296Thr
ENST00000398788.4:c.151C>A	ENSP00000381768.3:p.Pro51Thr
ENST00000475158.1:n.407C>A
ENST00000619887.4:c.151C>A	ENSP00000478374.1:p.Pro51Thr
ENST00000622827.4:c.6871C>A	ENSP00000483211.1:p.Pro2291Thr
NM_001171933.1:c.151C>A	NP_001165404.1:p.Pro51Thr
NM_001171934.1:c.151C>A	NP_001165405.1:p.Pro51Thr
NM_022124.5:c.6871C>A	NP_071407.4:p.Pro2291Thr
XM_006717940.2:c.7066C>A	XP_006718003.1:p.Pro2356Thr
XM_006717942.2:c.7000C>A	XP_006718005.1:p.Pro2334Thr
XM_011540039.1:c.7063C>A	XP_011538341.1:p.Pro2355Thr
XM_011540040.1:c.7060C>A	XP_011538342.1:p.Pro2354Thr
XM_011540041.1:c.7006C>A	XP_011538343.1:p.Pro2336Thr
XM_011540042.1:c.6976C>A	XP_011538344.1:p.Pro2326Thr
XM_011540043.1:c.7066C>A	XP_011538345.1:p.Pro2356Thr
XM_011540044.1:c.6931C>A	XP_011538346.1:p.Pro2311Thr
XM_011540045.1:c.7066C>A	XP_011538347.1:p.Pro2356Thr
XM_011540046.1:c.6526C>A	XP_011538348.1:p.Pro2176Thr
XM_011540047.1:c.5884C>A	XP_011538349.1:p.Pro1962Thr
XM_011540052.1:c.3394C>A	XP_011538354.1:p.Pro1132Thr
NM_022124.6:c.6871C>A MANE Select	NP_071407.4:p.Pro2291Thr