Canonical Allele Identifier: CA377162327

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73565949G>C (hg19) ; chr10:g.71806192G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71806192G>C , CM000672.2:g.71806192G>C	GRCh38
NC_000010.10:g.73565949G>C , CM000672.1:g.73565949G>C	GRCh37
NC_000010.9:g.73235955G>C	NCBI36
NG_008835.1:g.414246G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.8089G>C MANE Select	ENSP00000224721.9:p.Gly2697Arg
ENST00000642965.1:c.2022G>C	ENSP00000495222.1:n.2022G>C
ENST00000647092.1:c.1686G>C	ENSP00000495176.1:n.1686G>C
ENST00000224721.10:c.8104G>C	ENSP00000224721.8:p.Gly2702Arg
ENST00000398788.4:c.1369G>C	ENSP00000381768.3:p.Gly457Arg
ENST00000475158.1:n.1625G>C
ENST00000619887.4:c.1369G>C	ENSP00000478374.1:p.Gly457Arg
ENST00000622827.4:c.8089G>C	ENSP00000483211.1:p.Gly2697Arg
NM_001171933.1:c.1369G>C	NP_001165404.1:p.Gly457Arg
NM_001171934.1:c.1369G>C	NP_001165405.1:p.Gly457Arg
NM_022124.5:c.8089G>C	NP_071407.4:p.Gly2697Arg
XM_006717940.2:c.8284G>C	XP_006718003.1:p.Gly2762Arg
XM_006717942.2:c.8218G>C	XP_006718005.1:p.Gly2740Arg
XM_011540039.1:c.8281G>C	XP_011538341.1:p.Gly2761Arg
XM_011540040.1:c.8278G>C	XP_011538342.1:p.Gly2760Arg
XM_011540041.1:c.8224G>C	XP_011538343.1:p.Gly2742Arg
XM_011540042.1:c.8194G>C	XP_011538344.1:p.Gly2732Arg
XM_011540043.1:c.8284G>C	XP_011538345.1:p.Gly2762Arg
XM_011540044.1:c.8149G>C	XP_011538346.1:p.Gly2717Arg
XM_011540045.1:c.8284G>C	XP_011538347.1:p.Gly2762Arg
XM_011540046.1:c.7744G>C	XP_011538348.1:p.Gly2582Arg
XM_011540047.1:c.7102G>C	XP_011538349.1:p.Gly2368Arg
XM_011540052.1:c.4612G>C	XP_011538354.1:p.Gly1538Arg
NM_022124.6:c.8089G>C MANE Select	NP_071407.4:p.Gly2697Arg