Canonical Allele Identifier: CA377160909

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73562808T>A (hg19) ; chr10:g.71803051T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71803051T>A , CM000672.2:g.71803051T>A	GRCh38
NC_000010.10:g.73562808T>A , CM000672.1:g.73562808T>A	GRCh37
NC_000010.9:g.73232814T>A	NCBI36
NG_008835.1:g.411105T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7636T>A MANE Select	ENSP00000224721.9:p.Tyr2546Asn
ENST00000642965.1:c.1569T>A	ENSP00000495222.1:n.1569T>A
ENST00000647092.1:c.1233T>A	ENSP00000495176.1:n.1233T>A
ENST00000224721.10:c.7651T>A	ENSP00000224721.8:p.Tyr2551Asn
ENST00000398788.4:c.916T>A	ENSP00000381768.3:p.Tyr306Asn
ENST00000475158.1:n.1172T>A
ENST00000619887.4:c.916T>A	ENSP00000478374.1:p.Tyr306Asn
ENST00000622827.4:c.7636T>A	ENSP00000483211.1:p.Tyr2546Asn
NM_001171933.1:c.916T>A	NP_001165404.1:p.Tyr306Asn
NM_001171934.1:c.916T>A	NP_001165405.1:p.Tyr306Asn
NM_022124.5:c.7636T>A	NP_071407.4:p.Tyr2546Asn
XM_006717940.2:c.7831T>A	XP_006718003.1:p.Tyr2611Asn
XM_006717942.2:c.7765T>A	XP_006718005.1:p.Tyr2589Asn
XM_011540039.1:c.7828T>A	XP_011538341.1:p.Tyr2610Asn
XM_011540040.1:c.7825T>A	XP_011538342.1:p.Tyr2609Asn
XM_011540041.1:c.7771T>A	XP_011538343.1:p.Tyr2591Asn
XM_011540042.1:c.7741T>A	XP_011538344.1:p.Tyr2581Asn
XM_011540043.1:c.7831T>A	XP_011538345.1:p.Tyr2611Asn
XM_011540044.1:c.7696T>A	XP_011538346.1:p.Tyr2566Asn
XM_011540045.1:c.7831T>A	XP_011538347.1:p.Tyr2611Asn
XM_011540046.1:c.7291T>A	XP_011538348.1:p.Tyr2431Asn
XM_011540047.1:c.6649T>A	XP_011538349.1:p.Tyr2217Asn
XM_011540052.1:c.4159T>A	XP_011538354.1:p.Tyr1387Asn
NM_022124.6:c.7636T>A MANE Select	NP_071407.4:p.Tyr2546Asn