Canonical Allele Identifier: CA1918870427

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71790415T= , CM000672.2:g.71790415T=	GRCh38
NC_000010.10:g.73550172T= , CM000672.1:g.73550172T=	GRCh37
NC_000010.9:g.73220178T=	NCBI36
NG_008835.1:g.398469T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6049+2T= MANE Select	ENSP00000224721.9:n.6049+2T=
ENST00000224721.10:c.6064+2T=	ENSP00000224721.8:n.6064+2T=
ENST00000622827.4:c.6049+2T=	ENSP00000483211.1:n.6049+2T=
NM_022124.5:c.6049+2T=	NP_071407.4:n.6049+2T=
XM_006717940.2:c.6244+2T=	XP_006718003.1:n.6244+2T=
XM_006717942.2:c.6178+2T=	XP_006718005.1:n.6178+2T=
XM_011540039.1:c.6241+2T=	XP_011538341.1:n.6241+2T=
XM_011540040.1:c.6238+2T=	XP_011538342.1:n.6238+2T=
XM_011540041.1:c.6184+2T=	XP_011538343.1:n.6184+2T=
XM_011540042.1:c.6244+2T=	XP_011538344.1:n.6244+2T=
XM_011540043.1:c.6244+2T=	XP_011538345.1:n.6244+2T=
XM_011540044.1:c.6109+2T=	XP_011538346.1:n.6109+2T=
XM_011540045.1:c.6244+2T=	XP_011538347.1:n.6244+2T=
XM_011540046.1:c.5704+2T=	XP_011538348.1:n.5704+2T=
XM_011540047.1:c.5062+2T=	XP_011538349.1:n.5062+2T=
XM_011540048.1:c.6244+2T=	XP_011538350.1:n.6244+2T=
XM_011540049.1:c.6244+2T=	XP_011538351.1:n.6244+2T=
XM_011540050.1:c.6244+2T=	XP_011538352.1:n.6244+2T=
XM_011540051.1:c.6244+2T=	XP_011538353.1:n.6244+2T=
XM_011540052.1:c.2572+2T=	XP_011538354.1:n.2572+2T=
XR_945796.1:n.6487+2T=
NM_022124.6:c.6049+2T= MANE Select	NP_071407.4:n.6049+2T=