Canonical Allele Identifier: CA182096

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71815239C>T , CM000672.2:g.71815239C>T	GRCh38
NC_000010.10:g.73574996C>T , CM000672.1:g.73574996C>T	GRCh37
NC_000010.9:g.73245002C>T	NCBI36
NG_008835.1:g.423293C>T
NG_009301.1:g.41087G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_022124.6:c.10026C>T MANE Select	NP_071407.4:p.Asp3342=
ENST00000224721.12:c.10026C>T MANE Select	ENSP00000224721.9:p.Asp3342=
NM_001171933.1:c.3306C>T	NP_001165404.1:p.Asp1102=
NM_001171934.1:c.3201C>T	NP_001165405.1:p.Asp1067=
NM_001171935.1:c.717C>T	NP_001165406.1:p.Asp239=
NM_001171936.1:c.612C>T	NP_001165407.1:p.Asp204=
NM_022124.5:c.10026C>T	NP_071407.4:p.Asp3342=
ENST00000224721.10:c.10041C>T	ENSP00000224721.8:p.Asp3347=
ENST00000398788.4:c.3306C>T	ENSP00000381768.3:p.Asp1102=
ENST00000475158.1:n.3457C>T
ENST00000619887.4:c.3201C>T	ENSP00000478374.1:p.Asp1067=
ENST00000622827.4:c.10026C>T	ENSP00000483211.1:p.Asp3342=
ENST00000642965.1:c.3959C>T	ENSP00000495222.1:n.3959C>T
ENST00000647092.1:c.3518C>T	ENSP00000495176.1:n.3518C>T
XM_006717940.2:c.10221C>T	XP_006718003.1:p.Asp3407=
XM_006717942.2:c.10155C>T	XP_006718005.1:p.Asp3385=
XM_011540039.1:c.10218C>T	XP_011538341.1:p.Asp3406=
XM_011540040.1:c.10215C>T	XP_011538342.1:p.Asp3405=
XM_011540041.1:c.10161C>T	XP_011538343.1:p.Asp3387=
XM_011540042.1:c.10131C>T	XP_011538344.1:p.Asp3377=
XM_011540043.1:c.10116C>T	XP_011538345.1:p.Asp3372=
XM_011540044.1:c.10086C>T	XP_011538346.1:p.Asp3362=
XM_011540046.1:c.9681C>T	XP_011538348.1:p.Asp3227=
XM_011540047.1:c.9039C>T	XP_011538349.1:p.Asp3013=
XM_011540052.1:c.6549C>T	XP_011538354.1:p.Asp2183=