Canonical Allele Identifier: CA1918871526

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71791215G= , CM000672.2:g.71791215G=	GRCh38
NC_000010.10:g.73550972G= , CM000672.1:g.73550972G=	GRCh37
NC_000010.9:g.73220978G=	NCBI36
NG_008835.1:g.399269G=

Transcript Alleles

HGVS	Amino-acid Change
NM_022124.6:c.6133G= MANE Select	NP_071407.4:p.Asp2045=
ENST00000224721.12:c.6133G= MANE Select	ENSP00000224721.9:p.Asp2045=
NM_022124.5:c.6133G=	NP_071407.4:p.Asp2045=
ENST00000224721.10:c.6148G=	ENSP00000224721.8:p.Asp2050=
ENST00000622827.4:c.6133G=	ENSP00000483211.1:p.Asp2045=
XM_006717940.2:c.6328G=	XP_006718003.1:p.Asp2110=
XM_006717942.2:c.6262G=	XP_006718005.1:p.Asp2088=
XM_011540039.1:c.6325G=	XP_011538341.1:p.Asp2109=
XM_011540040.1:c.6322G=	XP_011538342.1:p.Asp2108=
XM_011540041.1:c.6268G=	XP_011538343.1:p.Asp2090=
XM_011540042.1:c.6328G=	XP_011538344.1:p.Asp2110=
XM_011540043.1:c.6328G=	XP_011538345.1:p.Asp2110=
XM_011540044.1:c.6193G=	XP_011538346.1:p.Asp2065=
XM_011540045.1:c.6328G=	XP_011538347.1:p.Asp2110=
XM_011540046.1:c.5788G=	XP_011538348.1:p.Asp1930=
XM_011540047.1:c.5146G=	XP_011538349.1:p.Asp1716=
XM_011540048.1:c.6328G=	XP_011538350.1:p.Asp2110=
XM_011540049.1:c.6328G=	XP_011538351.1:p.Asp2110=
XM_011540050.1:c.6328G=	XP_011538352.1:p.Asp2110=
XM_011540051.1:c.6328G=	XP_011538353.1:p.Asp2110=
XM_011540052.1:c.2656G=	XP_011538354.1:p.Asp886=
XR_945796.1:n.6571G=