Canonical Allele Identifier: CA470062237

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73560404T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71800647T>C , CM000672.2:g.71800647T>C	GRCh38
NC_000010.10:g.73560404T>C , CM000672.1:g.73560404T>C	GRCh37
NC_000010.9:g.73230410T>C	NCBI36
NG_008835.1:g.408701T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7374T>C MANE Select	ENSP00000224721.9:p.Tyr2458=
ENST00000642965.1:c.1307T>C	ENSP00000495222.1:n.1307T>C
ENST00000647092.1:c.971T>C	ENSP00000495176.1:n.971T>C
ENST00000224721.10:c.7389T>C	ENSP00000224721.8:p.Tyr2463=
ENST00000398788.4:c.654T>C	ENSP00000381768.3:p.Tyr218=
ENST00000475158.1:n.910T>C
ENST00000619887.4:c.654T>C	ENSP00000478374.1:p.Tyr218=
ENST00000622827.4:c.7374T>C	ENSP00000483211.1:p.Tyr2458=
NM_001171933.1:c.654T>C	NP_001165404.1:p.Tyr218=
NM_001171934.1:c.654T>C	NP_001165405.1:p.Tyr218=
NM_022124.5:c.7374T>C	NP_071407.4:p.Tyr2458=
XM_006717940.2:c.7569T>C	XP_006718003.1:p.Tyr2523=
XM_006717942.2:c.7503T>C	XP_006718005.1:p.Tyr2501=
XM_011540039.1:c.7566T>C	XP_011538341.1:p.Tyr2522=
XM_011540040.1:c.7563T>C	XP_011538342.1:p.Tyr2521=
XM_011540041.1:c.7509T>C	XP_011538343.1:p.Tyr2503=
XM_011540042.1:c.7479T>C	XP_011538344.1:p.Tyr2493=
XM_011540043.1:c.7569T>C	XP_011538345.1:p.Tyr2523=
XM_011540044.1:c.7434T>C	XP_011538346.1:p.Tyr2478=
XM_011540045.1:c.7569T>C	XP_011538347.1:p.Tyr2523=
XM_011540046.1:c.7029T>C	XP_011538348.1:p.Tyr2343=
XM_011540047.1:c.6387T>C	XP_011538349.1:p.Tyr2129=
XM_011540052.1:c.3897T>C	XP_011538354.1:p.Tyr1299=
NM_022124.6:c.7374T>C MANE Select	NP_071407.4:p.Tyr2458=