Canonical Allele Identifier: CA377159962

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73560468A>G (hg19) ; chr10:g.71800711A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71800711A>G , CM000672.2:g.71800711A>G	GRCh38
NC_000010.10:g.73560468A>G , CM000672.1:g.73560468A>G	GRCh37
NC_000010.9:g.73230474A>G	NCBI36
NG_008835.1:g.408765A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7438A>G MANE Select	ENSP00000224721.9:p.Asn2480Asp
ENST00000642965.1:c.1371A>G	ENSP00000495222.1:n.1371A>G
ENST00000647092.1:c.1035A>G	ENSP00000495176.1:n.1035A>G
ENST00000224721.10:c.7453A>G	ENSP00000224721.8:p.Asn2485Asp
ENST00000398788.4:c.718A>G	ENSP00000381768.3:p.Asn240Asp
ENST00000475158.1:n.974A>G
ENST00000619887.4:c.718A>G	ENSP00000478374.1:p.Asn240Asp
ENST00000622827.4:c.7438A>G	ENSP00000483211.1:p.Asn2480Asp
NM_001171933.1:c.718A>G	NP_001165404.1:p.Asn240Asp
NM_001171934.1:c.718A>G	NP_001165405.1:p.Asn240Asp
NM_022124.5:c.7438A>G	NP_071407.4:p.Asn2480Asp
XM_006717940.2:c.7633A>G	XP_006718003.1:p.Asn2545Asp
XM_006717942.2:c.7567A>G	XP_006718005.1:p.Asn2523Asp
XM_011540039.1:c.7630A>G	XP_011538341.1:p.Asn2544Asp
XM_011540040.1:c.7627A>G	XP_011538342.1:p.Asn2543Asp
XM_011540041.1:c.7573A>G	XP_011538343.1:p.Asn2525Asp
XM_011540042.1:c.7543A>G	XP_011538344.1:p.Asn2515Asp
XM_011540043.1:c.7633A>G	XP_011538345.1:p.Asn2545Asp
XM_011540044.1:c.7498A>G	XP_011538346.1:p.Asn2500Asp
XM_011540045.1:c.7633A>G	XP_011538347.1:p.Asn2545Asp
XM_011540046.1:c.7093A>G	XP_011538348.1:p.Asn2365Asp
XM_011540047.1:c.6451A>G	XP_011538349.1:p.Asn2151Asp
XM_011540052.1:c.3961A>G	XP_011538354.1:p.Asn1321Asp
NM_022124.6:c.7438A>G MANE Select	NP_071407.4:p.Asn2480Asp