Canonical Allele Identifier: CA1918874092

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793143G= , CM000672.2:g.71793143G=	GRCh38
NC_000010.10:g.73552900G= , CM000672.1:g.73552900G=	GRCh37
NC_000010.9:g.73222906G=	NCBI36
NG_008835.1:g.401197G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6254-39G= MANE Select	ENSP00000224721.9:n.6254-39G=
ENST00000224721.10:c.6269-39G=	ENSP00000224721.8:n.6269-39G=
ENST00000622827.4:c.6254-39G=	ENSP00000483211.1:n.6254-39G=
NM_022124.5:c.6254-39G=	NP_071407.4:n.6254-39G=
XM_006717940.2:c.6449-39G=	XP_006718003.1:n.6449-39G=
XM_006717942.2:c.6383-39G=	XP_006718005.1:n.6383-39G=
XM_011540039.1:c.6446-39G=	XP_011538341.1:n.6446-39G=
XM_011540040.1:c.6443-39G=	XP_011538342.1:n.6443-39G=
XM_011540041.1:c.6389-39G=	XP_011538343.1:n.6389-39G=
XM_011540042.1:c.6449-39G=	XP_011538344.1:n.6449-39G=
XM_011540043.1:c.6449-39G=	XP_011538345.1:n.6449-39G=
XM_011540044.1:c.6314-39G=	XP_011538346.1:n.6314-39G=
XM_011540045.1:c.6449-39G=	XP_011538347.1:n.6449-39G=
XM_011540046.1:c.5909-39G=	XP_011538348.1:n.5909-39G=
XM_011540047.1:c.5267-39G=	XP_011538349.1:n.5267-39G=
XM_011540048.1:c.6449-39G=	XP_011538350.1:n.6449-39G=
XM_011540049.1:c.6449-39G=	XP_011538351.1:n.6449-39G=
XM_011540050.1:c.6449-39G=	XP_011538352.1:n.6449-39G=
XM_011540051.1:c.6449-39G=	XP_011538353.1:n.6449-39G=
XM_011540052.1:c.2777-39G=	XP_011538354.1:n.2777-39G=
XR_945796.1:n.6692-39G=
NM_022124.6:c.6254-39G= MANE Select	NP_071407.4:n.6254-39G=