Canonical Allele Identifier: CA377160464

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73500623C>G (hg19) ; chr10:g.71740866C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740866C>G , CM000672.2:g.71740866C>G	GRCh38
NC_000010.10:g.73500623C>G , CM000672.1:g.73500623C>G	GRCh37
NC_000010.9:g.73170629C>G	NCBI36
NG_008835.1:g.348920C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4533C>G MANE Select	ENSP00000224721.9:p.His1511Gln
ENST00000224721.10:c.4548C>G	ENSP00000224721.8:p.His1516Gln
ENST00000398792.3:n.1222C>G
ENST00000622827.4:c.4533C>G	ENSP00000483211.1:p.His1511Gln
NM_022124.5:c.4533C>G	NP_071407.4:p.His1511Gln
XM_006717940.2:c.4728C>G	XP_006718003.1:p.His1576Gln
XM_006717942.2:c.4662C>G	XP_006718005.1:p.His1554Gln
XM_011540039.1:c.4725C>G	XP_011538341.1:p.His1575Gln
XM_011540040.1:c.4722C>G	XP_011538342.1:p.His1574Gln
XM_011540041.1:c.4668C>G	XP_011538343.1:p.His1556Gln
XM_011540042.1:c.4728C>G	XP_011538344.1:p.His1576Gln
XM_011540043.1:c.4728C>G	XP_011538345.1:p.His1576Gln
XM_011540044.1:c.4593C>G	XP_011538346.1:p.His1531Gln
XM_011540045.1:c.4728C>G	XP_011538347.1:p.His1576Gln
XM_011540046.1:c.4188C>G	XP_011538348.1:p.His1396Gln
XM_011540047.1:c.3546C>G	XP_011538349.1:p.His1182Gln
XM_011540048.1:c.4728C>G	XP_011538350.1:p.His1576Gln
XM_011540049.1:c.4728C>G	XP_011538351.1:p.His1576Gln
XM_011540050.1:c.4728C>G	XP_011538352.1:p.His1576Gln
XM_011540051.1:c.4728C>G	XP_011538353.1:p.His1576Gln
XM_011540052.1:c.1056C>G	XP_011538354.1:p.His352Gln
XM_011540053.1:c.4728C>G	XP_011538355.1:p.His1576Gln
XR_945796.1:n.4971C>G
NM_022124.6:c.4533C>G MANE Select	NP_071407.4:p.His1511Gln