Canonical Allele Identifier: CA1918874283

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793348C= , CM000672.2:g.71793348C=	GRCh38
NC_000010.10:g.73553105C= , CM000672.1:g.73553105C=	GRCh37
NC_000010.9:g.73223111C=	NCBI36
NG_008835.1:g.401402C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6420C= MANE Select	ENSP00000224721.9:p.Tyr2140=
ENST00000224721.10:c.6435C=	ENSP00000224721.8:p.Tyr2145=
ENST00000622827.4:c.6420C=	ENSP00000483211.1:p.Tyr2140=
NM_022124.5:c.6420C=	NP_071407.4:p.Tyr2140=
XM_006717940.2:c.6615C=	XP_006718003.1:p.Tyr2205=
XM_006717942.2:c.6549C=	XP_006718005.1:p.Tyr2183=
XM_011540039.1:c.6612C=	XP_011538341.1:p.Tyr2204=
XM_011540040.1:c.6609C=	XP_011538342.1:p.Tyr2203=
XM_011540041.1:c.6555C=	XP_011538343.1:p.Tyr2185=
XM_011540042.1:c.6577+38C=	XP_011538344.1:n.6577+38C=
XM_011540043.1:c.6615C=	XP_011538345.1:p.Tyr2205=
XM_011540044.1:c.6480C=	XP_011538346.1:p.Tyr2160=
XM_011540045.1:c.6615C=	XP_011538347.1:p.Tyr2205=
XM_011540046.1:c.6075C=	XP_011538348.1:p.Tyr2025=
XM_011540047.1:c.5433C=	XP_011538349.1:p.Tyr1811=
XM_011540048.1:c.6615C=	XP_011538350.1:p.Tyr2205=
XM_011540049.1:c.6615C=	XP_011538351.1:p.Tyr2205=
XM_011540050.1:c.6615C=	XP_011538352.1:p.Tyr2205=
XM_011540051.1:c.6615C=	XP_011538353.1:p.Tyr2205=
XM_011540052.1:c.2943C=	XP_011538354.1:p.Tyr981=
XR_945796.1:n.6858C=
NM_022124.6:c.6420C= MANE Select	NP_071407.4:p.Tyr2140=