Canonical Allele Identifier: CA377160625

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73562734A>T (hg19) ; chr10:g.71802977A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71802977A>T , CM000672.2:g.71802977A>T	GRCh38
NC_000010.10:g.73562734A>T , CM000672.1:g.73562734A>T	GRCh37
NC_000010.9:g.73232740A>T	NCBI36
NG_008835.1:g.411031A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7562A>T MANE Select	ENSP00000224721.9:p.Asn2521Ile
ENST00000642965.1:c.1495A>T	ENSP00000495222.1:n.1495A>T
ENST00000647092.1:c.1159A>T	ENSP00000495176.1:n.1159A>T
ENST00000224721.10:c.7577A>T	ENSP00000224721.8:p.Asn2526Ile
ENST00000398788.4:c.842A>T	ENSP00000381768.3:p.Asn281Ile
ENST00000475158.1:n.1098A>T
ENST00000619887.4:c.842A>T	ENSP00000478374.1:p.Asn281Ile
ENST00000622827.4:c.7562A>T	ENSP00000483211.1:p.Asn2521Ile
NM_001171933.1:c.842A>T	NP_001165404.1:p.Asn281Ile
NM_001171934.1:c.842A>T	NP_001165405.1:p.Asn281Ile
NM_022124.5:c.7562A>T	NP_071407.4:p.Asn2521Ile
XM_006717940.2:c.7757A>T	XP_006718003.1:p.Asn2586Ile
XM_006717942.2:c.7691A>T	XP_006718005.1:p.Asn2564Ile
XM_011540039.1:c.7754A>T	XP_011538341.1:p.Asn2585Ile
XM_011540040.1:c.7751A>T	XP_011538342.1:p.Asn2584Ile
XM_011540041.1:c.7697A>T	XP_011538343.1:p.Asn2566Ile
XM_011540042.1:c.7667A>T	XP_011538344.1:p.Asn2556Ile
XM_011540043.1:c.7757A>T	XP_011538345.1:p.Asn2586Ile
XM_011540044.1:c.7622A>T	XP_011538346.1:p.Asn2541Ile
XM_011540045.1:c.7757A>T	XP_011538347.1:p.Asn2586Ile
XM_011540046.1:c.7217A>T	XP_011538348.1:p.Asn2406Ile
XM_011540047.1:c.6575A>T	XP_011538349.1:p.Asn2192Ile
XM_011540052.1:c.4085A>T	XP_011538354.1:p.Asn1362Ile
NM_022124.6:c.7562A>T MANE Select	NP_071407.4:p.Asn2521Ile