Canonical Allele Identifier: CA377160664

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73562743C>G (hg19) ; chr10:g.71802986C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71802986C>G , CM000672.2:g.71802986C>G	GRCh38
NC_000010.10:g.73562743C>G , CM000672.1:g.73562743C>G	GRCh37
NC_000010.9:g.73232749C>G	NCBI36
NG_008835.1:g.411040C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7571C>G MANE Select	ENSP00000224721.9:p.Ala2524Gly
ENST00000642965.1:c.1504C>G	ENSP00000495222.1:n.1504C>G
ENST00000647092.1:c.1168C>G	ENSP00000495176.1:n.1168C>G
ENST00000224721.10:c.7586C>G	ENSP00000224721.8:p.Ala2529Gly
ENST00000398788.4:c.851C>G	ENSP00000381768.3:p.Ala284Gly
ENST00000475158.1:n.1107C>G
ENST00000619887.4:c.851C>G	ENSP00000478374.1:p.Ala284Gly
ENST00000622827.4:c.7571C>G	ENSP00000483211.1:p.Ala2524Gly
NM_001171933.1:c.851C>G	NP_001165404.1:p.Ala284Gly
NM_001171934.1:c.851C>G	NP_001165405.1:p.Ala284Gly
NM_022124.5:c.7571C>G	NP_071407.4:p.Ala2524Gly
XM_006717940.2:c.7766C>G	XP_006718003.1:p.Ala2589Gly
XM_006717942.2:c.7700C>G	XP_006718005.1:p.Ala2567Gly
XM_011540039.1:c.7763C>G	XP_011538341.1:p.Ala2588Gly
XM_011540040.1:c.7760C>G	XP_011538342.1:p.Ala2587Gly
XM_011540041.1:c.7706C>G	XP_011538343.1:p.Ala2569Gly
XM_011540042.1:c.7676C>G	XP_011538344.1:p.Ala2559Gly
XM_011540043.1:c.7766C>G	XP_011538345.1:p.Ala2589Gly
XM_011540044.1:c.7631C>G	XP_011538346.1:p.Ala2544Gly
XM_011540045.1:c.7766C>G	XP_011538347.1:p.Ala2589Gly
XM_011540046.1:c.7226C>G	XP_011538348.1:p.Ala2409Gly
XM_011540047.1:c.6584C>G	XP_011538349.1:p.Ala2195Gly
XM_011540052.1:c.4094C>G	XP_011538354.1:p.Ala1365Gly
NM_022124.6:c.7571C>G MANE Select	NP_071407.4:p.Ala2524Gly