Canonical Allele Identifier: CA137433
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45949
dbSNP Id: rs10999978

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71740842C>T , CM000672.2:g.71740842C>T GRCh38
NC_000010.10:g.73500599C>T , CM000672.1:g.73500599C>T GRCh37
NC_000010.9:g.73170605C>T NCBI36
NG_008835.1:g.348896C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.4509C>T MANE Select ENSP00000224721.9:p.Gly1503=
ENST00000224721.10:c.4524C>T ENSP00000224721.8:p.Gly1508=
ENST00000398792.3:n.1198C>T
ENST00000622827.4:c.4509C>T ENSP00000483211.1:p.Gly1503=
NM_022124.5:c.4509C>T NP_071407.4:p.Gly1503=
XM_006717940.2:c.4704C>T XP_006718003.1:p.Gly1568=
XM_006717942.2:c.4638C>T XP_006718005.1:p.Gly1546=
XM_011540039.1:c.4701C>T XP_011538341.1:p.Gly1567=
XM_011540040.1:c.4698C>T XP_011538342.1:p.Gly1566=
XM_011540041.1:c.4644C>T XP_011538343.1:p.Gly1548=
XM_011540042.1:c.4704C>T XP_011538344.1:p.Gly1568=
XM_011540043.1:c.4704C>T XP_011538345.1:p.Gly1568=
XM_011540044.1:c.4569C>T XP_011538346.1:p.Gly1523=
XM_011540045.1:c.4704C>T XP_011538347.1:p.Gly1568=
XM_011540046.1:c.4164C>T XP_011538348.1:p.Gly1388=
XM_011540047.1:c.3522C>T XP_011538349.1:p.Gly1174=
XM_011540048.1:c.4704C>T XP_011538350.1:p.Gly1568=
XM_011540049.1:c.4704C>T XP_011538351.1:p.Gly1568=
XM_011540050.1:c.4704C>T XP_011538352.1:p.Gly1568=
XM_011540051.1:c.4704C>T XP_011538353.1:p.Gly1568=
XM_011540052.1:c.1032C>T XP_011538354.1:p.Gly344=
XM_011540053.1:c.4704C>T XP_011538355.1:p.Gly1568=
XR_945796.1:n.4947C>T
NM_022124.6:c.4509C>T MANE Select NP_071407.4:p.Gly1503=