Canonical Allele Identifier: CA1918862180

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71784935T= , CM000672.2:g.71784935T=	GRCh38
NC_000010.10:g.73544692T= , CM000672.1:g.73544692T=	GRCh37
NC_000010.9:g.73214698T=	NCBI36
NG_008835.1:g.392989T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5547T= MANE Select	ENSP00000224721.9:p.Pro1849=
ENST00000224721.10:c.5562T=	ENSP00000224721.8:p.Pro1854=
ENST00000622827.4:c.5547T=	ENSP00000483211.1:p.Pro1849=
NM_022124.5:c.5547T=	NP_071407.4:p.Pro1849=
XM_006717940.2:c.5742T=	XP_006718003.1:p.Pro1914=
XM_006717942.2:c.5676T=	XP_006718005.1:p.Pro1892=
XM_011540039.1:c.5739T=	XP_011538341.1:p.Pro1913=
XM_011540040.1:c.5736T=	XP_011538342.1:p.Pro1912=
XM_011540041.1:c.5682T=	XP_011538343.1:p.Pro1894=
XM_011540042.1:c.5742T=	XP_011538344.1:p.Pro1914=
XM_011540043.1:c.5742T=	XP_011538345.1:p.Pro1914=
XM_011540044.1:c.5607T=	XP_011538346.1:p.Pro1869=
XM_011540045.1:c.5742T=	XP_011538347.1:p.Pro1914=
XM_011540046.1:c.5202T=	XP_011538348.1:p.Pro1734=
XM_011540047.1:c.4560T=	XP_011538349.1:p.Pro1520=
XM_011540048.1:c.5742T=	XP_011538350.1:p.Pro1914=
XM_011540049.1:c.5742T=	XP_011538351.1:p.Pro1914=
XM_011540050.1:c.5742T=	XP_011538352.1:p.Pro1914=
XM_011540051.1:c.5742T=	XP_011538353.1:p.Pro1914=
XM_011540052.1:c.2070T=	XP_011538354.1:p.Pro690=
XM_011540053.1:c.5742T=	XP_011538355.1:p.Pro1914=
XR_945796.1:n.5985T=
NM_022124.6:c.5547T= MANE Select	NP_071407.4:p.Pro1849=