Canonical Allele Identifier: CA470069232

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73500653T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740896T>C , CM000672.2:g.71740896T>C	GRCh38
NC_000010.10:g.73500653T>C , CM000672.1:g.73500653T>C	GRCh37
NC_000010.9:g.73170659T>C	NCBI36
NG_008835.1:g.348950T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4563T>C MANE Select	ENSP00000224721.9:p.Asn1521=
ENST00000224721.10:c.4578T>C	ENSP00000224721.8:p.Asn1526=
ENST00000398792.3:n.1252T>C
ENST00000622827.4:c.4563T>C	ENSP00000483211.1:p.Asn1521=
NM_022124.5:c.4563T>C	NP_071407.4:p.Asn1521=
XM_006717940.2:c.4758T>C	XP_006718003.1:p.Asn1586=
XM_006717942.2:c.4692T>C	XP_006718005.1:p.Asn1564=
XM_011540039.1:c.4755T>C	XP_011538341.1:p.Asn1585=
XM_011540040.1:c.4752T>C	XP_011538342.1:p.Asn1584=
XM_011540041.1:c.4698T>C	XP_011538343.1:p.Asn1566=
XM_011540042.1:c.4758T>C	XP_011538344.1:p.Asn1586=
XM_011540043.1:c.4758T>C	XP_011538345.1:p.Asn1586=
XM_011540044.1:c.4623T>C	XP_011538346.1:p.Asn1541=
XM_011540045.1:c.4758T>C	XP_011538347.1:p.Asn1586=
XM_011540046.1:c.4218T>C	XP_011538348.1:p.Asn1406=
XM_011540047.1:c.3576T>C	XP_011538349.1:p.Asn1192=
XM_011540048.1:c.4758T>C	XP_011538350.1:p.Asn1586=
XM_011540049.1:c.4758T>C	XP_011538351.1:p.Asn1586=
XM_011540050.1:c.4758T>C	XP_011538352.1:p.Asn1586=
XM_011540051.1:c.4758T>C	XP_011538353.1:p.Asn1586=
XM_011540052.1:c.1086T>C	XP_011538354.1:p.Asn362=
XM_011540053.1:c.4758T>C	XP_011538355.1:p.Asn1586=
XR_945796.1:n.5001T>C
NM_022124.6:c.4563T>C MANE Select	NP_071407.4:p.Asn1521=