Canonical Allele Identifier: CA377155190

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73553182A>T (hg19) ; chr10:g.71793425A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793425A>T , CM000672.2:g.71793425A>T	GRCh38
NC_000010.10:g.73553182A>T , CM000672.1:g.73553182A>T	GRCh37
NC_000010.9:g.73223188A>T	NCBI36
NG_008835.1:g.401479A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6497A>T MANE Select	ENSP00000224721.9:p.Asp2166Val
ENST00000224721.10:c.6512A>T	ENSP00000224721.8:p.Asp2171Val
ENST00000622827.4:c.6497A>T	ENSP00000483211.1:p.Asp2166Val
NM_022124.5:c.6497A>T	NP_071407.4:p.Asp2166Val
XM_006717940.2:c.6692A>T	XP_006718003.1:p.Asp2231Val
XM_006717942.2:c.6626A>T	XP_006718005.1:p.Asp2209Val
XM_011540039.1:c.6689A>T	XP_011538341.1:p.Asp2230Val
XM_011540040.1:c.6686A>T	XP_011538342.1:p.Asp2229Val
XM_011540041.1:c.6632A>T	XP_011538343.1:p.Asp2211Val
XM_011540042.1:c.6602A>T	XP_011538344.1:p.Asp2201Val
XM_011540043.1:c.6692A>T	XP_011538345.1:p.Asp2231Val
XM_011540044.1:c.6557A>T	XP_011538346.1:p.Asp2186Val
XM_011540045.1:c.6692A>T	XP_011538347.1:p.Asp2231Val
XM_011540046.1:c.6152A>T	XP_011538348.1:p.Asp2051Val
XM_011540047.1:c.5510A>T	XP_011538349.1:p.Asp1837Val
XM_011540048.1:c.6692A>T	XP_011538350.1:p.Asp2231Val
XM_011540049.1:c.6692A>T	XP_011538351.1:p.Asp2231Val
XM_011540050.1:c.6692A>T	XP_011538352.1:p.Asp2231Val
XM_011540051.1:c.6692A>T	XP_011538353.1:p.Asp2231Val
XM_011540052.1:c.3020A>T	XP_011538354.1:p.Asp1007Val
XR_945796.1:n.6935A>T
NM_022124.6:c.6497A>T MANE Select	NP_071407.4:p.Asp2166Val