Canonical Allele Identifier: CA377160637

Gene: CDH23

Linked Data

• dbSNP Id: rs1839717249
• gnomAD v3: 10-71740906-C-T
• gnomAD v4: 10-71740906-C-T
• MyVariant Identifiers: chr10:g.73500663C>T (hg19) ; chr10:g.71740906C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740906C>T , CM000672.2:g.71740906C>T	GRCh38
NC_000010.10:g.73500663C>T , CM000672.1:g.73500663C>T	GRCh37
NC_000010.9:g.73170669C>T	NCBI36
NG_008835.1:g.348960C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4573C>T MANE Select	ENSP00000224721.9:p.Pro1525Ser
ENST00000224721.10:c.4588C>T	ENSP00000224721.8:p.Pro1530Ser
ENST00000398792.3:n.1262C>T
ENST00000622827.4:c.4573C>T	ENSP00000483211.1:p.Pro1525Ser
NM_022124.5:c.4573C>T	NP_071407.4:p.Pro1525Ser
XM_006717940.2:c.4768C>T	XP_006718003.1:p.Pro1590Ser
XM_006717942.2:c.4702C>T	XP_006718005.1:p.Pro1568Ser
XM_011540039.1:c.4765C>T	XP_011538341.1:p.Pro1589Ser
XM_011540040.1:c.4762C>T	XP_011538342.1:p.Pro1588Ser
XM_011540041.1:c.4708C>T	XP_011538343.1:p.Pro1570Ser
XM_011540042.1:c.4768C>T	XP_011538344.1:p.Pro1590Ser
XM_011540043.1:c.4768C>T	XP_011538345.1:p.Pro1590Ser
XM_011540044.1:c.4633C>T	XP_011538346.1:p.Pro1545Ser
XM_011540045.1:c.4768C>T	XP_011538347.1:p.Pro1590Ser
XM_011540046.1:c.4228C>T	XP_011538348.1:p.Pro1410Ser
XM_011540047.1:c.3586C>T	XP_011538349.1:p.Pro1196Ser
XM_011540048.1:c.4768C>T	XP_011538350.1:p.Pro1590Ser
XM_011540049.1:c.4768C>T	XP_011538351.1:p.Pro1590Ser
XM_011540050.1:c.4768C>T	XP_011538352.1:p.Pro1590Ser
XM_011540051.1:c.4768C>T	XP_011538353.1:p.Pro1590Ser
XM_011540052.1:c.1096C>T	XP_011538354.1:p.Pro366Ser
XM_011540053.1:c.4768C>T	XP_011538355.1:p.Pro1590Ser
XR_945796.1:n.5011C>T
NM_022124.6:c.4573C>T MANE Select	NP_071407.4:p.Pro1525Ser