Canonical Allele Identifier: CA377146783

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73544763T>G (hg19) ; chr10:g.71785006T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71785006T>G , CM000672.2:g.71785006T>G	GRCh38
NC_000010.10:g.73544763T>G , CM000672.1:g.73544763T>G	GRCh37
NC_000010.9:g.73214769T>G	NCBI36
NG_008835.1:g.393060T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.5618T>G MANE Select	ENSP00000224721.9:p.Val1873Gly
ENST00000224721.10:c.5633T>G	ENSP00000224721.8:p.Val1878Gly
ENST00000622827.4:c.5618T>G	ENSP00000483211.1:p.Val1873Gly
NM_022124.5:c.5618T>G	NP_071407.4:p.Val1873Gly
XM_006717940.2:c.5813T>G	XP_006718003.1:p.Val1938Gly
XM_006717942.2:c.5747T>G	XP_006718005.1:p.Val1916Gly
XM_011540039.1:c.5810T>G	XP_011538341.1:p.Val1937Gly
XM_011540040.1:c.5807T>G	XP_011538342.1:p.Val1936Gly
XM_011540041.1:c.5753T>G	XP_011538343.1:p.Val1918Gly
XM_011540042.1:c.5813T>G	XP_011538344.1:p.Val1938Gly
XM_011540043.1:c.5813T>G	XP_011538345.1:p.Val1938Gly
XM_011540044.1:c.5678T>G	XP_011538346.1:p.Val1893Gly
XM_011540045.1:c.5813T>G	XP_011538347.1:p.Val1938Gly
XM_011540046.1:c.5273T>G	XP_011538348.1:p.Val1758Gly
XM_011540047.1:c.4631T>G	XP_011538349.1:p.Val1544Gly
XM_011540048.1:c.5813T>G	XP_011538350.1:p.Val1938Gly
XM_011540049.1:c.5813T>G	XP_011538351.1:p.Val1938Gly
XM_011540050.1:c.5813T>G	XP_011538352.1:p.Val1938Gly
XM_011540051.1:c.5813T>G	XP_011538353.1:p.Val1938Gly
XM_011540052.1:c.2141T>G	XP_011538354.1:p.Val714Gly
XM_011540053.1:c.5813T>G	XP_011538355.1:p.Val1938Gly
XR_945796.1:n.6056T>G
NM_022124.6:c.5618T>G MANE Select	NP_071407.4:p.Val1873Gly