Canonical Allele Identifier: CA470062055

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73558232T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798475T>G , CM000672.2:g.71798475T>G	GRCh38
NC_000010.10:g.73558232T>G , CM000672.1:g.73558232T>G	GRCh37
NC_000010.9:g.73228238T>G	NCBI36
NG_008835.1:g.406529T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6951T>G MANE Select	ENSP00000224721.9:p.Ala2317=
ENST00000642965.1:c.884T>G	ENSP00000495222.1:n.884T>G
ENST00000647092.1:c.548T>G	ENSP00000495176.1:n.548T>G
ENST00000224721.10:c.6966T>G	ENSP00000224721.8:p.Ala2322=
ENST00000398788.4:c.231T>G	ENSP00000381768.3:p.Ala77=
ENST00000475158.1:n.487T>G
ENST00000619887.4:c.231T>G	ENSP00000478374.1:p.Ala77=
ENST00000622827.4:c.6951T>G	ENSP00000483211.1:p.Ala2317=
NM_001171933.1:c.231T>G	NP_001165404.1:p.Ala77=
NM_001171934.1:c.231T>G	NP_001165405.1:p.Ala77=
NM_022124.5:c.6951T>G	NP_071407.4:p.Ala2317=
XM_006717940.2:c.7146T>G	XP_006718003.1:p.Ala2382=
XM_006717942.2:c.7080T>G	XP_006718005.1:p.Ala2360=
XM_011540039.1:c.7143T>G	XP_011538341.1:p.Ala2381=
XM_011540040.1:c.7140T>G	XP_011538342.1:p.Ala2380=
XM_011540041.1:c.7086T>G	XP_011538343.1:p.Ala2362=
XM_011540042.1:c.7056T>G	XP_011538344.1:p.Ala2352=
XM_011540043.1:c.7146T>G	XP_011538345.1:p.Ala2382=
XM_011540044.1:c.7011T>G	XP_011538346.1:p.Ala2337=
XM_011540045.1:c.7146T>G	XP_011538347.1:p.Ala2382=
XM_011540046.1:c.6606T>G	XP_011538348.1:p.Ala2202=
XM_011540047.1:c.5964T>G	XP_011538349.1:p.Ala1988=
XM_011540052.1:c.3474T>G	XP_011538354.1:p.Ala1158=
NM_022124.6:c.6951T>G MANE Select	NP_071407.4:p.Ala2317=