Canonical Allele Identifier: CA377160375

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73500601C>A (hg19) ; chr10:g.71740844C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740844C>A , CM000672.2:g.71740844C>A	GRCh38
NC_000010.10:g.73500601C>A , CM000672.1:g.73500601C>A	GRCh37
NC_000010.9:g.73170607C>A	NCBI36
NG_008835.1:g.348898C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.4511C>A MANE Select	ENSP00000224721.9:p.Thr1504Asn
ENST00000224721.10:c.4526C>A	ENSP00000224721.8:p.Thr1509Asn
ENST00000398792.3:n.1200C>A
ENST00000622827.4:c.4511C>A	ENSP00000483211.1:p.Thr1504Asn
NM_022124.5:c.4511C>A	NP_071407.4:p.Thr1504Asn
XM_006717940.2:c.4706C>A	XP_006718003.1:p.Thr1569Asn
XM_006717942.2:c.4640C>A	XP_006718005.1:p.Thr1547Asn
XM_011540039.1:c.4703C>A	XP_011538341.1:p.Thr1568Asn
XM_011540040.1:c.4700C>A	XP_011538342.1:p.Thr1567Asn
XM_011540041.1:c.4646C>A	XP_011538343.1:p.Thr1549Asn
XM_011540042.1:c.4706C>A	XP_011538344.1:p.Thr1569Asn
XM_011540043.1:c.4706C>A	XP_011538345.1:p.Thr1569Asn
XM_011540044.1:c.4571C>A	XP_011538346.1:p.Thr1524Asn
XM_011540045.1:c.4706C>A	XP_011538347.1:p.Thr1569Asn
XM_011540046.1:c.4166C>A	XP_011538348.1:p.Thr1389Asn
XM_011540047.1:c.3524C>A	XP_011538349.1:p.Thr1175Asn
XM_011540048.1:c.4706C>A	XP_011538350.1:p.Thr1569Asn
XM_011540049.1:c.4706C>A	XP_011538351.1:p.Thr1569Asn
XM_011540050.1:c.4706C>A	XP_011538352.1:p.Thr1569Asn
XM_011540051.1:c.4706C>A	XP_011538353.1:p.Thr1569Asn
XM_011540052.1:c.1034C>A	XP_011538354.1:p.Thr345Asn
XM_011540053.1:c.4706C>A	XP_011538355.1:p.Thr1569Asn
XR_945796.1:n.4949C>A
NM_022124.6:c.4511C>A MANE Select	NP_071407.4:p.Thr1504Asn