Canonical Allele Identifier: CA377131284

Gene: CDH23

Linked Data

• dbSNP Id: rs2132988617
• MyVariant Identifiers: chr10:g.73567273C>T (hg19) ; chr10:g.71807516C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71807516C>T , CM000672.2:g.71807516C>T	GRCh38
NC_000010.10:g.73567273C>T , CM000672.1:g.73567273C>T	GRCh37
NC_000010.9:g.73237279C>T	NCBI36
NG_008835.1:g.415570C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.8309C>T MANE Select	ENSP00000224721.9:p.Ala2770Val
ENST00000642965.1:c.2242C>T	ENSP00000495222.1:n.2242C>T
ENST00000647092.1:c.1906C>T	ENSP00000495176.1:n.1906C>T
ENST00000224721.10:c.8324C>T	ENSP00000224721.8:p.Ala2775Val
ENST00000398788.4:c.1589C>T	ENSP00000381768.3:p.Ala530Val
ENST00000475158.1:n.1845C>T
ENST00000619887.4:c.1589C>T	ENSP00000478374.1:p.Ala530Val
ENST00000622827.4:c.8309C>T	ENSP00000483211.1:p.Ala2770Val
NM_001171933.1:c.1589C>T	NP_001165404.1:p.Ala530Val
NM_001171934.1:c.1589C>T	NP_001165405.1:p.Ala530Val
NM_022124.5:c.8309C>T	NP_071407.4:p.Ala2770Val
XM_006717940.2:c.8504C>T	XP_006718003.1:p.Ala2835Val
XM_006717942.2:c.8438C>T	XP_006718005.1:p.Ala2813Val
XM_011540039.1:c.8501C>T	XP_011538341.1:p.Ala2834Val
XM_011540040.1:c.8498C>T	XP_011538342.1:p.Ala2833Val
XM_011540041.1:c.8444C>T	XP_011538343.1:p.Ala2815Val
XM_011540042.1:c.8414C>T	XP_011538344.1:p.Ala2805Val
XM_011540043.1:c.8504C>T	XP_011538345.1:p.Ala2835Val
XM_011540044.1:c.8369C>T	XP_011538346.1:p.Ala2790Val
XM_011540045.1:c.8504C>T	XP_011538347.1:p.Ala2835Val
XM_011540046.1:c.7964C>T	XP_011538348.1:p.Ala2655Val
XM_011540047.1:c.7322C>T	XP_011538349.1:p.Ala2441Val
XM_011540052.1:c.4832C>T	XP_011538354.1:p.Ala1611Val
NM_022124.6:c.8309C>T MANE Select	NP_071407.4:p.Ala2770Val