Canonical Allele Identifier: CA470062482

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73562735T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71802978T>C , CM000672.2:g.71802978T>C	GRCh38
NC_000010.10:g.73562735T>C , CM000672.1:g.73562735T>C	GRCh37
NC_000010.9:g.73232741T>C	NCBI36
NG_008835.1:g.411032T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7563T>C MANE Select	ENSP00000224721.9:p.Asn2521=
ENST00000642965.1:c.1496T>C	ENSP00000495222.1:n.1496T>C
ENST00000647092.1:c.1160T>C	ENSP00000495176.1:n.1160T>C
ENST00000224721.10:c.7578T>C	ENSP00000224721.8:p.Asn2526=
ENST00000398788.4:c.843T>C	ENSP00000381768.3:p.Asn281=
ENST00000475158.1:n.1099T>C
ENST00000619887.4:c.843T>C	ENSP00000478374.1:p.Asn281=
ENST00000622827.4:c.7563T>C	ENSP00000483211.1:p.Asn2521=
NM_001171933.1:c.843T>C	NP_001165404.1:p.Asn281=
NM_001171934.1:c.843T>C	NP_001165405.1:p.Asn281=
NM_022124.5:c.7563T>C	NP_071407.4:p.Asn2521=
XM_006717940.2:c.7758T>C	XP_006718003.1:p.Asn2586=
XM_006717942.2:c.7692T>C	XP_006718005.1:p.Asn2564=
XM_011540039.1:c.7755T>C	XP_011538341.1:p.Asn2585=
XM_011540040.1:c.7752T>C	XP_011538342.1:p.Asn2584=
XM_011540041.1:c.7698T>C	XP_011538343.1:p.Asn2566=
XM_011540042.1:c.7668T>C	XP_011538344.1:p.Asn2556=
XM_011540043.1:c.7758T>C	XP_011538345.1:p.Asn2586=
XM_011540044.1:c.7623T>C	XP_011538346.1:p.Asn2541=
XM_011540045.1:c.7758T>C	XP_011538347.1:p.Asn2586=
XM_011540046.1:c.7218T>C	XP_011538348.1:p.Asn2406=
XM_011540047.1:c.6576T>C	XP_011538349.1:p.Asn2192=
XM_011540052.1:c.4086T>C	XP_011538354.1:p.Asn1362=
NM_022124.6:c.7563T>C MANE Select	NP_071407.4:p.Asn2521=