Canonical Allele Identifier: CA5545816

Gene: CDH23

Linked Data

• dbSNP Id: rs775411358
• ExAC: 10:73544759 C / T
• gnomAD v2: 10-73544759-C-T
• gnomAD v4: 10-71785002-C-T
• MyVariant Identifiers: chr10:g.73544759C>T (hg19) ; chr10:g.71785002C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71785002C>T , CM000672.2:g.71785002C>T	GRCh38
NC_000010.10:g.73544759C>T , CM000672.1:g.73544759C>T	GRCh37
NC_000010.9:g.73214765C>T	NCBI36
NG_008835.1:g.393056C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5614C>T MANE Select	ENSP00000224721.9:p.His1872Tyr
ENST00000224721.10:c.5629C>T	ENSP00000224721.8:p.His1877Tyr
ENST00000622827.4:c.5614C>T	ENSP00000483211.1:p.His1872Tyr
NM_022124.5:c.5614C>T	NP_071407.4:p.His1872Tyr
XM_006717940.2:c.5809C>T	XP_006718003.1:p.His1937Tyr
XM_006717942.2:c.5743C>T	XP_006718005.1:p.His1915Tyr
XM_011540039.1:c.5806C>T	XP_011538341.1:p.His1936Tyr
XM_011540040.1:c.5803C>T	XP_011538342.1:p.His1935Tyr
XM_011540041.1:c.5749C>T	XP_011538343.1:p.His1917Tyr
XM_011540042.1:c.5809C>T	XP_011538344.1:p.His1937Tyr
XM_011540043.1:c.5809C>T	XP_011538345.1:p.His1937Tyr
XM_011540044.1:c.5674C>T	XP_011538346.1:p.His1892Tyr
XM_011540045.1:c.5809C>T	XP_011538347.1:p.His1937Tyr
XM_011540046.1:c.5269C>T	XP_011538348.1:p.His1757Tyr
XM_011540047.1:c.4627C>T	XP_011538349.1:p.His1543Tyr
XM_011540048.1:c.5809C>T	XP_011538350.1:p.His1937Tyr
XM_011540049.1:c.5809C>T	XP_011538351.1:p.His1937Tyr
XM_011540050.1:c.5809C>T	XP_011538352.1:p.His1937Tyr
XM_011540051.1:c.5809C>T	XP_011538353.1:p.His1937Tyr
XM_011540052.1:c.2137C>T	XP_011538354.1:p.His713Tyr
XM_011540053.1:c.5809C>T	XP_011538355.1:p.His1937Tyr
XR_945796.1:n.6052C>T
NM_022124.6:c.5614C>T MANE Select	NP_071407.4:p.His1872Tyr