Canonical Allele Identifier: CA2722285582

Gene: CDH23

Linked Data

• dbSNP Id: rs2132953414

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793264T>A , CM000672.2:g.71793264T>A	GRCh38
NC_000010.10:g.73553021T>A , CM000672.1:g.73553021T>A	GRCh37
NC_000010.9:g.73223027T>A	NCBI36
NG_008835.1:g.401318T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6336T>A MANE Select	ENSP00000224721.9:p.Ala2112=
ENST00000224721.10:c.6351T>A	ENSP00000224721.8:p.Ala2117=
ENST00000622827.4:c.6336T>A	ENSP00000483211.1:p.Ala2112=
NM_022124.5:c.6336T>A	NP_071407.4:p.Ala2112=
XM_006717940.2:c.6531T>A	XP_006718003.1:p.Ala2177=
XM_006717942.2:c.6465T>A	XP_006718005.1:p.Ala2155=
XM_011540039.1:c.6528T>A	XP_011538341.1:p.Ala2176=
XM_011540040.1:c.6525T>A	XP_011538342.1:p.Ala2175=
XM_011540041.1:c.6471T>A	XP_011538343.1:p.Ala2157=
XM_011540042.1:c.6531T>A	XP_011538344.1:p.Ala2177=
XM_011540043.1:c.6531T>A	XP_011538345.1:p.Ala2177=
XM_011540044.1:c.6396T>A	XP_011538346.1:p.Ala2132=
XM_011540045.1:c.6531T>A	XP_011538347.1:p.Ala2177=
XM_011540046.1:c.5991T>A	XP_011538348.1:p.Ala1997=
XM_011540047.1:c.5349T>A	XP_011538349.1:p.Ala1783=
XM_011540048.1:c.6531T>A	XP_011538350.1:p.Ala2177=
XM_011540049.1:c.6531T>A	XP_011538351.1:p.Ala2177=
XM_011540050.1:c.6531T>A	XP_011538352.1:p.Ala2177=
XM_011540051.1:c.6531T>A	XP_011538353.1:p.Ala2177=
XM_011540052.1:c.2859T>A	XP_011538354.1:p.Ala953=
XR_945796.1:n.6774T>A
NM_022124.6:c.6336T>A MANE Select	NP_071407.4:p.Ala2112=