Canonical Allele Identifier: CA377158170

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73558265T>G (hg19) ; chr10:g.71798508T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798508T>G , CM000672.2:g.71798508T>G	GRCh38
NC_000010.10:g.73558265T>G , CM000672.1:g.73558265T>G	GRCh37
NC_000010.9:g.73228271T>G	NCBI36
NG_008835.1:g.406562T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6984T>G MANE Select	ENSP00000224721.9:p.Asn2328Lys
ENST00000642965.1:c.917T>G	ENSP00000495222.1:n.917T>G
ENST00000647092.1:c.581T>G	ENSP00000495176.1:n.581T>G
ENST00000224721.10:c.6999T>G	ENSP00000224721.8:p.Asn2333Lys
ENST00000398788.4:c.264T>G	ENSP00000381768.3:p.Asn88Lys
ENST00000475158.1:n.520T>G
ENST00000619887.4:c.264T>G	ENSP00000478374.1:p.Asn88Lys
ENST00000622827.4:c.6984T>G	ENSP00000483211.1:p.Asn2328Lys
NM_001171933.1:c.264T>G	NP_001165404.1:p.Asn88Lys
NM_001171934.1:c.264T>G	NP_001165405.1:p.Asn88Lys
NM_022124.5:c.6984T>G	NP_071407.4:p.Asn2328Lys
XM_006717940.2:c.7179T>G	XP_006718003.1:p.Asn2393Lys
XM_006717942.2:c.7113T>G	XP_006718005.1:p.Asn2371Lys
XM_011540039.1:c.7176T>G	XP_011538341.1:p.Asn2392Lys
XM_011540040.1:c.7173T>G	XP_011538342.1:p.Asn2391Lys
XM_011540041.1:c.7119T>G	XP_011538343.1:p.Asn2373Lys
XM_011540042.1:c.7089T>G	XP_011538344.1:p.Asn2363Lys
XM_011540043.1:c.7179T>G	XP_011538345.1:p.Asn2393Lys
XM_011540044.1:c.7044T>G	XP_011538346.1:p.Asn2348Lys
XM_011540045.1:c.7179T>G	XP_011538347.1:p.Asn2393Lys
XM_011540046.1:c.6639T>G	XP_011538348.1:p.Asn2213Lys
XM_011540047.1:c.5997T>G	XP_011538349.1:p.Asn1999Lys
XM_011540052.1:c.3507T>G	XP_011538354.1:p.Asn1169Lys
NM_022124.6:c.6984T>G MANE Select	NP_071407.4:p.Asn2328Lys