Canonical Allele Identifier: CA377146868

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73544781A>T (hg19) ; chr10:g.71785024A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71785024A>T , CM000672.2:g.71785024A>T	GRCh38
NC_000010.10:g.73544781A>T , CM000672.1:g.73544781A>T	GRCh37
NC_000010.9:g.73214787A>T	NCBI36
NG_008835.1:g.393078A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5636A>T MANE Select	ENSP00000224721.9:p.Asp1879Val
ENST00000224721.10:c.5651A>T	ENSP00000224721.8:p.Asp1884Val
ENST00000622827.4:c.5636A>T	ENSP00000483211.1:p.Asp1879Val
NM_022124.5:c.5636A>T	NP_071407.4:p.Asp1879Val
XM_006717940.2:c.5831A>T	XP_006718003.1:p.Asp1944Val
XM_006717942.2:c.5765A>T	XP_006718005.1:p.Asp1922Val
XM_011540039.1:c.5828A>T	XP_011538341.1:p.Asp1943Val
XM_011540040.1:c.5825A>T	XP_011538342.1:p.Asp1942Val
XM_011540041.1:c.5771A>T	XP_011538343.1:p.Asp1924Val
XM_011540042.1:c.5831A>T	XP_011538344.1:p.Asp1944Val
XM_011540043.1:c.5831A>T	XP_011538345.1:p.Asp1944Val
XM_011540044.1:c.5696A>T	XP_011538346.1:p.Asp1899Val
XM_011540045.1:c.5831A>T	XP_011538347.1:p.Asp1944Val
XM_011540046.1:c.5291A>T	XP_011538348.1:p.Asp1764Val
XM_011540047.1:c.4649A>T	XP_011538349.1:p.Asp1550Val
XM_011540048.1:c.5831A>T	XP_011538350.1:p.Asp1944Val
XM_011540049.1:c.5831A>T	XP_011538351.1:p.Asp1944Val
XM_011540050.1:c.5831A>T	XP_011538352.1:p.Asp1944Val
XM_011540051.1:c.5831A>T	XP_011538353.1:p.Asp1944Val
XM_011540052.1:c.2159A>T	XP_011538354.1:p.Asp720Val
XM_011540053.1:c.5831A>T	XP_011538355.1:p.Asp1944Val
XR_945796.1:n.6074A>T
NM_022124.6:c.5636A>T MANE Select	NP_071407.4:p.Asp1879Val