Canonical Allele Identifier: CA1918874465

Gene: CDH23

Linked Data

• dbSNP Id: rs1841317518

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793426C>T , CM000672.2:g.71793426C>T	GRCh38
NC_000010.10:g.73553183C>T , CM000672.1:g.73553183C>T	GRCh37
NC_000010.9:g.73223189C>T	NCBI36
NG_008835.1:g.401480C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6498C>T MANE Select	ENSP00000224721.9:p.Asp2166=
ENST00000224721.10:c.6513C>T	ENSP00000224721.8:p.Asp2171=
ENST00000622827.4:c.6498C>T	ENSP00000483211.1:p.Asp2166=
NM_022124.5:c.6498C>T	NP_071407.4:p.Asp2166=
XM_006717940.2:c.6693C>T	XP_006718003.1:p.Asp2231=
XM_006717942.2:c.6627C>T	XP_006718005.1:p.Asp2209=
XM_011540039.1:c.6690C>T	XP_011538341.1:p.Asp2230=
XM_011540040.1:c.6687C>T	XP_011538342.1:p.Asp2229=
XM_011540041.1:c.6633C>T	XP_011538343.1:p.Asp2211=
XM_011540042.1:c.6603C>T	XP_011538344.1:p.Asp2201=
XM_011540043.1:c.6693C>T	XP_011538345.1:p.Asp2231=
XM_011540044.1:c.6558C>T	XP_011538346.1:p.Asp2186=
XM_011540045.1:c.6693C>T	XP_011538347.1:p.Asp2231=
XM_011540046.1:c.6153C>T	XP_011538348.1:p.Asp2051=
XM_011540047.1:c.5511C>T	XP_011538349.1:p.Asp1837=
XM_011540048.1:c.6693C>T	XP_011538350.1:p.Asp2231=
XM_011540049.1:c.6693C>T	XP_011538351.1:p.Asp2231=
XM_011540050.1:c.6693C>T	XP_011538352.1:p.Asp2231=
XM_011540051.1:c.6693C>T	XP_011538353.1:p.Asp2231=
XM_011540052.1:c.3021C>T	XP_011538354.1:p.Asp1007=
XR_945796.1:n.6936C>T
NM_022124.6:c.6498C>T MANE Select	NP_071407.4:p.Asp2166=