Canonical Allele Identifier: CA377160616

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73562733A>G (hg19) ; chr10:g.71802976A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71802976A>G , CM000672.2:g.71802976A>G	GRCh38
NC_000010.10:g.73562733A>G , CM000672.1:g.73562733A>G	GRCh37
NC_000010.9:g.73232739A>G	NCBI36
NG_008835.1:g.411030A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7561A>G MANE Select	ENSP00000224721.9:p.Asn2521Asp
ENST00000642965.1:c.1494A>G	ENSP00000495222.1:n.1494A>G
ENST00000647092.1:c.1158A>G	ENSP00000495176.1:n.1158A>G
ENST00000224721.10:c.7576A>G	ENSP00000224721.8:p.Asn2526Asp
ENST00000398788.4:c.841A>G	ENSP00000381768.3:p.Asn281Asp
ENST00000475158.1:n.1097A>G
ENST00000619887.4:c.841A>G	ENSP00000478374.1:p.Asn281Asp
ENST00000622827.4:c.7561A>G	ENSP00000483211.1:p.Asn2521Asp
NM_001171933.1:c.841A>G	NP_001165404.1:p.Asn281Asp
NM_001171934.1:c.841A>G	NP_001165405.1:p.Asn281Asp
NM_022124.5:c.7561A>G	NP_071407.4:p.Asn2521Asp
XM_006717940.2:c.7756A>G	XP_006718003.1:p.Asn2586Asp
XM_006717942.2:c.7690A>G	XP_006718005.1:p.Asn2564Asp
XM_011540039.1:c.7753A>G	XP_011538341.1:p.Asn2585Asp
XM_011540040.1:c.7750A>G	XP_011538342.1:p.Asn2584Asp
XM_011540041.1:c.7696A>G	XP_011538343.1:p.Asn2566Asp
XM_011540042.1:c.7666A>G	XP_011538344.1:p.Asn2556Asp
XM_011540043.1:c.7756A>G	XP_011538345.1:p.Asn2586Asp
XM_011540044.1:c.7621A>G	XP_011538346.1:p.Asn2541Asp
XM_011540045.1:c.7756A>G	XP_011538347.1:p.Asn2586Asp
XM_011540046.1:c.7216A>G	XP_011538348.1:p.Asn2406Asp
XM_011540047.1:c.6574A>G	XP_011538349.1:p.Asn2192Asp
XM_011540052.1:c.4084A>G	XP_011538354.1:p.Asn1362Asp
NM_022124.6:c.7561A>G MANE Select	NP_071407.4:p.Asn2521Asp