Canonical Allele Identifier: CA377158320

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73558291A>T (hg19) ; chr10:g.71798534A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71798534A>T , CM000672.2:g.71798534A>T	GRCh38
NC_000010.10:g.73558291A>T , CM000672.1:g.73558291A>T	GRCh37
NC_000010.9:g.73228297A>T	NCBI36
NG_008835.1:g.406588A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7010A>T MANE Select	ENSP00000224721.9:p.Asp2337Val
ENST00000642965.1:c.943A>T	ENSP00000495222.1:n.943A>T
ENST00000647092.1:c.607A>T	ENSP00000495176.1:n.607A>T
ENST00000224721.10:c.7025A>T	ENSP00000224721.8:p.Asp2342Val
ENST00000398788.4:c.290A>T	ENSP00000381768.3:p.Asp97Val
ENST00000475158.1:n.546A>T
ENST00000619887.4:c.290A>T	ENSP00000478374.1:p.Asp97Val
ENST00000622827.4:c.7010A>T	ENSP00000483211.1:p.Asp2337Val
NM_001171933.1:c.290A>T	NP_001165404.1:p.Asp97Val
NM_001171934.1:c.290A>T	NP_001165405.1:p.Asp97Val
NM_022124.5:c.7010A>T	NP_071407.4:p.Asp2337Val
XM_006717940.2:c.7205A>T	XP_006718003.1:p.Asp2402Val
XM_006717942.2:c.7139A>T	XP_006718005.1:p.Asp2380Val
XM_011540039.1:c.7202A>T	XP_011538341.1:p.Asp2401Val
XM_011540040.1:c.7199A>T	XP_011538342.1:p.Asp2400Val
XM_011540041.1:c.7145A>T	XP_011538343.1:p.Asp2382Val
XM_011540042.1:c.7115A>T	XP_011538344.1:p.Asp2372Val
XM_011540043.1:c.7205A>T	XP_011538345.1:p.Asp2402Val
XM_011540044.1:c.7070A>T	XP_011538346.1:p.Asp2357Val
XM_011540045.1:c.7205A>T	XP_011538347.1:p.Asp2402Val
XM_011540046.1:c.6665A>T	XP_011538348.1:p.Asp2222Val
XM_011540047.1:c.6023A>T	XP_011538349.1:p.Asp2008Val
XM_011540052.1:c.3533A>T	XP_011538354.1:p.Asp1178Val
NM_022124.6:c.7010A>T MANE Select	NP_071407.4:p.Asp2337Val