Canonical Allele Identifier: CA377160456

Gene: CDH23

Linked Data

• dbSNP Id: rs776890902
• MyVariant Identifiers: chr10:g.73500621C>T (hg19) ; chr10:g.71740864C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740864C>T , CM000672.2:g.71740864C>T	GRCh38
NC_000010.10:g.73500621C>T , CM000672.1:g.73500621C>T	GRCh37
NC_000010.9:g.73170627C>T	NCBI36
NG_008835.1:g.348918C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.4531C>T MANE Select	ENSP00000224721.9:p.His1511Tyr
ENST00000224721.10:c.4546C>T	ENSP00000224721.8:p.His1516Tyr
ENST00000398792.3:n.1220C>T
ENST00000622827.4:c.4531C>T	ENSP00000483211.1:p.His1511Tyr
NM_022124.5:c.4531C>T	NP_071407.4:p.His1511Tyr
XM_006717940.2:c.4726C>T	XP_006718003.1:p.His1576Tyr
XM_006717942.2:c.4660C>T	XP_006718005.1:p.His1554Tyr
XM_011540039.1:c.4723C>T	XP_011538341.1:p.His1575Tyr
XM_011540040.1:c.4720C>T	XP_011538342.1:p.His1574Tyr
XM_011540041.1:c.4666C>T	XP_011538343.1:p.His1556Tyr
XM_011540042.1:c.4726C>T	XP_011538344.1:p.His1576Tyr
XM_011540043.1:c.4726C>T	XP_011538345.1:p.His1576Tyr
XM_011540044.1:c.4591C>T	XP_011538346.1:p.His1531Tyr
XM_011540045.1:c.4726C>T	XP_011538347.1:p.His1576Tyr
XM_011540046.1:c.4186C>T	XP_011538348.1:p.His1396Tyr
XM_011540047.1:c.3544C>T	XP_011538349.1:p.His1182Tyr
XM_011540048.1:c.4726C>T	XP_011538350.1:p.His1576Tyr
XM_011540049.1:c.4726C>T	XP_011538351.1:p.His1576Tyr
XM_011540050.1:c.4726C>T	XP_011538352.1:p.His1576Tyr
XM_011540051.1:c.4726C>T	XP_011538353.1:p.His1576Tyr
XM_011540052.1:c.1054C>T	XP_011538354.1:p.His352Tyr
XM_011540053.1:c.4726C>T	XP_011538355.1:p.His1576Tyr
XR_945796.1:n.4969C>T
NM_022124.6:c.4531C>T MANE Select	NP_071407.4:p.His1511Tyr