Canonical Allele Identifier: CA1918853835

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740852C= , CM000672.2:g.71740852C=	GRCh38
NC_000010.10:g.73500609C= , CM000672.1:g.73500609C=	GRCh37
NC_000010.9:g.73170615C=	NCBI36
NG_008835.1:g.348906C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.4519C= MANE Select	ENSP00000224721.9:p.Arg1507=
ENST00000224721.10:c.4534C=	ENSP00000224721.8:p.Arg1512=
ENST00000398792.3:n.1208C=
ENST00000622827.4:c.4519C=	ENSP00000483211.1:p.Arg1507=
NM_022124.5:c.4519C=	NP_071407.4:p.Arg1507=
XM_006717940.2:c.4714C=	XP_006718003.1:p.Arg1572=
XM_006717942.2:c.4648C=	XP_006718005.1:p.Arg1550=
XM_011540039.1:c.4711C=	XP_011538341.1:p.Arg1571=
XM_011540040.1:c.4708C=	XP_011538342.1:p.Arg1570=
XM_011540041.1:c.4654C=	XP_011538343.1:p.Arg1552=
XM_011540042.1:c.4714C=	XP_011538344.1:p.Arg1572=
XM_011540043.1:c.4714C=	XP_011538345.1:p.Arg1572=
XM_011540044.1:c.4579C=	XP_011538346.1:p.Arg1527=
XM_011540045.1:c.4714C=	XP_011538347.1:p.Arg1572=
XM_011540046.1:c.4174C=	XP_011538348.1:p.Arg1392=
XM_011540047.1:c.3532C=	XP_011538349.1:p.Arg1178=
XM_011540048.1:c.4714C=	XP_011538350.1:p.Arg1572=
XM_011540049.1:c.4714C=	XP_011538351.1:p.Arg1572=
XM_011540050.1:c.4714C=	XP_011538352.1:p.Arg1572=
XM_011540051.1:c.4714C=	XP_011538353.1:p.Arg1572=
XM_011540052.1:c.1042C=	XP_011538354.1:p.Arg348=
XM_011540053.1:c.4714C=	XP_011538355.1:p.Arg1572=
XR_945796.1:n.4957C=
NM_022124.6:c.4519C= MANE Select	NP_071407.4:p.Arg1507=