Canonical Allele Identifier: CA5546147

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793606C>T , CM000672.2:g.71793606C>T	GRCh38
NC_000010.10:g.73553363C>T , CM000672.1:g.73553363C>T	GRCh37
NC_000010.9:g.73223369C>T	NCBI36
NG_008835.1:g.401660C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_022124.6:c.6678C>T MANE Select	NP_071407.4:p.Asn2226=
ENST00000224721.12:c.6678C>T MANE Select	ENSP00000224721.9:p.Asn2226=
NM_022124.5:c.6678C>T	NP_071407.4:p.Asn2226=
ENST00000224721.10:c.6693C>T	ENSP00000224721.8:p.Asn2231=
ENST00000622827.4:c.6678C>T	ENSP00000483211.1:p.Asn2226=
XM_006717940.2:c.6873C>T	XP_006718003.1:p.Asn2291=
XM_006717942.2:c.6807C>T	XP_006718005.1:p.Asn2269=
XM_011540039.1:c.6870C>T	XP_011538341.1:p.Asn2290=
XM_011540040.1:c.6867C>T	XP_011538342.1:p.Asn2289=
XM_011540041.1:c.6813C>T	XP_011538343.1:p.Asn2271=
XM_011540042.1:c.6783C>T	XP_011538344.1:p.Asn2261=
XM_011540043.1:c.6873C>T	XP_011538345.1:p.Asn2291=
XM_011540044.1:c.6738C>T	XP_011538346.1:p.Asn2246=
XM_011540045.1:c.6873C>T	XP_011538347.1:p.Asn2291=
XM_011540046.1:c.6333C>T	XP_011538348.1:p.Asn2111=
XM_011540047.1:c.5691C>T	XP_011538349.1:p.Asn1897=
XM_011540048.1:c.6873C>T	XP_011538350.1:p.Asn2291=
XM_011540049.1:c.6873C>T	XP_011538351.1:p.Asn2291=
XM_011540050.1:c.6873C>T	XP_011538352.1:p.Asn2291=
XM_011540051.1:c.6873C>T	XP_011538353.1:p.Asn2291=
XM_011540052.1:c.3201C>T	XP_011538354.1:p.Asn1067=
XR_945796.1:n.7116C>T