Canonical Allele Identifier: CA377153789

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73552941T>A (hg19) ; chr10:g.71793184T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793184T>A , CM000672.2:g.71793184T>A	GRCh38
NC_000010.10:g.73552941T>A , CM000672.1:g.73552941T>A	GRCh37
NC_000010.9:g.73222947T>A	NCBI36
NG_008835.1:g.401238T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6256T>A MANE Select	ENSP00000224721.9:p.Phe2086Ile
ENST00000224721.10:c.6271T>A	ENSP00000224721.8:p.Phe2091Ile
ENST00000622827.4:c.6256T>A	ENSP00000483211.1:p.Phe2086Ile
NM_022124.5:c.6256T>A	NP_071407.4:p.Phe2086Ile
XM_006717940.2:c.6451T>A	XP_006718003.1:p.Phe2151Ile
XM_006717942.2:c.6385T>A	XP_006718005.1:p.Phe2129Ile
XM_011540039.1:c.6448T>A	XP_011538341.1:p.Phe2150Ile
XM_011540040.1:c.6445T>A	XP_011538342.1:p.Phe2149Ile
XM_011540041.1:c.6391T>A	XP_011538343.1:p.Phe2131Ile
XM_011540042.1:c.6451T>A	XP_011538344.1:p.Phe2151Ile
XM_011540043.1:c.6451T>A	XP_011538345.1:p.Phe2151Ile
XM_011540044.1:c.6316T>A	XP_011538346.1:p.Phe2106Ile
XM_011540045.1:c.6451T>A	XP_011538347.1:p.Phe2151Ile
XM_011540046.1:c.5911T>A	XP_011538348.1:p.Phe1971Ile
XM_011540047.1:c.5269T>A	XP_011538349.1:p.Phe1757Ile
XM_011540048.1:c.6451T>A	XP_011538350.1:p.Phe2151Ile
XM_011540049.1:c.6451T>A	XP_011538351.1:p.Phe2151Ile
XM_011540050.1:c.6451T>A	XP_011538352.1:p.Phe2151Ile
XM_011540051.1:c.6451T>A	XP_011538353.1:p.Phe2151Ile
XM_011540052.1:c.2779T>A	XP_011538354.1:p.Phe927Ile
XR_945796.1:n.6694T>A
NM_022124.6:c.6256T>A MANE Select	NP_071407.4:p.Phe2086Ile