Canonical Allele Identifier: CA1918853832

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740845C= , CM000672.2:g.71740845C=	GRCh38
NC_000010.10:g.73500602C= , CM000672.1:g.73500602C=	GRCh37
NC_000010.9:g.73170608C=	NCBI36
NG_008835.1:g.348899C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.4512C= MANE Select	ENSP00000224721.9:p.Thr1504=
ENST00000224721.10:c.4527C=	ENSP00000224721.8:p.Thr1509=
ENST00000398792.3:n.1201C=
ENST00000622827.4:c.4512C=	ENSP00000483211.1:p.Thr1504=
NM_022124.5:c.4512C=	NP_071407.4:p.Thr1504=
XM_006717940.2:c.4707C=	XP_006718003.1:p.Thr1569=
XM_006717942.2:c.4641C=	XP_006718005.1:p.Thr1547=
XM_011540039.1:c.4704C=	XP_011538341.1:p.Thr1568=
XM_011540040.1:c.4701C=	XP_011538342.1:p.Thr1567=
XM_011540041.1:c.4647C=	XP_011538343.1:p.Thr1549=
XM_011540042.1:c.4707C=	XP_011538344.1:p.Thr1569=
XM_011540043.1:c.4707C=	XP_011538345.1:p.Thr1569=
XM_011540044.1:c.4572C=	XP_011538346.1:p.Thr1524=
XM_011540045.1:c.4707C=	XP_011538347.1:p.Thr1569=
XM_011540046.1:c.4167C=	XP_011538348.1:p.Thr1389=
XM_011540047.1:c.3525C=	XP_011538349.1:p.Thr1175=
XM_011540048.1:c.4707C=	XP_011538350.1:p.Thr1569=
XM_011540049.1:c.4707C=	XP_011538351.1:p.Thr1569=
XM_011540050.1:c.4707C=	XP_011538352.1:p.Thr1569=
XM_011540051.1:c.4707C=	XP_011538353.1:p.Thr1569=
XM_011540052.1:c.1035C=	XP_011538354.1:p.Thr345=
XM_011540053.1:c.4707C=	XP_011538355.1:p.Thr1569=
XR_945796.1:n.4950C=
NM_022124.6:c.4512C= MANE Select	NP_071407.4:p.Thr1504=