Canonical Allele Identifier: CA470060760

Gene: CDH23

Linked Data

• ClinVar Variation Id: 1651136
• ClinVar RCV Id: RCV002151560
• dbSNP Id: rs2132939321
• MyVariant Identifiers: chr10:g.73544770C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71785013C>T , CM000672.2:g.71785013C>T	GRCh38
NC_000010.10:g.73544770C>T , CM000672.1:g.73544770C>T	GRCh37
NC_000010.9:g.73214776C>T	NCBI36
NG_008835.1:g.393067C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5625C>T MANE Select	ENSP00000224721.9:p.Ala1875=
ENST00000224721.10:c.5640C>T	ENSP00000224721.8:p.Ala1880=
ENST00000622827.4:c.5625C>T	ENSP00000483211.1:p.Ala1875=
NM_022124.5:c.5625C>T	NP_071407.4:p.Ala1875=
XM_006717940.2:c.5820C>T	XP_006718003.1:p.Ala1940=
XM_006717942.2:c.5754C>T	XP_006718005.1:p.Ala1918=
XM_011540039.1:c.5817C>T	XP_011538341.1:p.Ala1939=
XM_011540040.1:c.5814C>T	XP_011538342.1:p.Ala1938=
XM_011540041.1:c.5760C>T	XP_011538343.1:p.Ala1920=
XM_011540042.1:c.5820C>T	XP_011538344.1:p.Ala1940=
XM_011540043.1:c.5820C>T	XP_011538345.1:p.Ala1940=
XM_011540044.1:c.5685C>T	XP_011538346.1:p.Ala1895=
XM_011540045.1:c.5820C>T	XP_011538347.1:p.Ala1940=
XM_011540046.1:c.5280C>T	XP_011538348.1:p.Ala1760=
XM_011540047.1:c.4638C>T	XP_011538349.1:p.Ala1546=
XM_011540048.1:c.5820C>T	XP_011538350.1:p.Ala1940=
XM_011540049.1:c.5820C>T	XP_011538351.1:p.Ala1940=
XM_011540050.1:c.5820C>T	XP_011538352.1:p.Ala1940=
XM_011540051.1:c.5820C>T	XP_011538353.1:p.Ala1940=
XM_011540052.1:c.2148C>T	XP_011538354.1:p.Ala716=
XM_011540053.1:c.5820C>T	XP_011538355.1:p.Ala1940=
XR_945796.1:n.6063C>T
NM_022124.6:c.5625C>T MANE Select	NP_071407.4:p.Ala1875=