Canonical Allele Identifier: CA377146755

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73544754T>A (hg19) ; chr10:g.71784997T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71784997T>A , CM000672.2:g.71784997T>A	GRCh38
NC_000010.10:g.73544754T>A , CM000672.1:g.73544754T>A	GRCh37
NC_000010.9:g.73214760T>A	NCBI36
NG_008835.1:g.393051T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5609T>A MANE Select	ENSP00000224721.9:p.Val1870Asp
ENST00000224721.10:c.5624T>A	ENSP00000224721.8:p.Val1875Asp
ENST00000622827.4:c.5609T>A	ENSP00000483211.1:p.Val1870Asp
NM_022124.5:c.5609T>A	NP_071407.4:p.Val1870Asp
XM_006717940.2:c.5804T>A	XP_006718003.1:p.Val1935Asp
XM_006717942.2:c.5738T>A	XP_006718005.1:p.Val1913Asp
XM_011540039.1:c.5801T>A	XP_011538341.1:p.Val1934Asp
XM_011540040.1:c.5798T>A	XP_011538342.1:p.Val1933Asp
XM_011540041.1:c.5744T>A	XP_011538343.1:p.Val1915Asp
XM_011540042.1:c.5804T>A	XP_011538344.1:p.Val1935Asp
XM_011540043.1:c.5804T>A	XP_011538345.1:p.Val1935Asp
XM_011540044.1:c.5669T>A	XP_011538346.1:p.Val1890Asp
XM_011540045.1:c.5804T>A	XP_011538347.1:p.Val1935Asp
XM_011540046.1:c.5264T>A	XP_011538348.1:p.Val1755Asp
XM_011540047.1:c.4622T>A	XP_011538349.1:p.Val1541Asp
XM_011540048.1:c.5804T>A	XP_011538350.1:p.Val1935Asp
XM_011540049.1:c.5804T>A	XP_011538351.1:p.Val1935Asp
XM_011540050.1:c.5804T>A	XP_011538352.1:p.Val1935Asp
XM_011540051.1:c.5804T>A	XP_011538353.1:p.Val1935Asp
XM_011540052.1:c.2132T>A	XP_011538354.1:p.Val711Asp
XM_011540053.1:c.5804T>A	XP_011538355.1:p.Val1935Asp
XR_945796.1:n.6047T>A
NM_022124.6:c.5609T>A MANE Select	NP_071407.4:p.Val1870Asp