Canonical Allele Identifier: CA377133415

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73447456T>G (hg19) ; chr10:g.71687699T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71687699T>G , CM000672.2:g.71687699T>G	GRCh38
NC_000010.10:g.73447456T>G , CM000672.1:g.73447456T>G	GRCh37
NC_000010.9:g.73117462T>G	NCBI36
NG_008835.1:g.295753T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.2039T>G MANE Select	ENSP00000224721.9:p.Val680Gly
ENST00000398809.9:c.2039T>G	ENSP00000381789.5:p.Val680Gly
ENST00000442677.4:c.2039T>G	ENSP00000388894.3:p.Val680Gly
ENST00000466757.8:c.1470T>G
ENST00000224721.10:c.2054T>G	ENSP00000224721.8:p.Val685Gly
ENST00000299366.11:c.2039T>G	ENSP00000299366.8:p.Val680Gly
ENST00000398809.8:c.2039T>G	ENSP00000381789.5:p.Val680Gly
ENST00000442677.3:c.814T>G
ENST00000466757.7:c.1470T>G
ENST00000616684.4:c.2039T>G	ENSP00000482036.2:p.Val680Gly
ENST00000622827.4:c.2039T>G	ENSP00000483211.1:p.Val680Gly
NM_001171930.1:c.2039T>G	NP_001165401.1:p.Val680Gly
NM_001171931.1:c.2039T>G	NP_001165402.1:p.Val680Gly
NM_022124.5:c.2039T>G	NP_071407.4:p.Val680Gly
XM_006717940.2:c.2234T>G	XP_006718003.1:p.Val745Gly
XM_006717942.2:c.2168T>G	XP_006718005.1:p.Val723Gly
XM_011540039.1:c.2234T>G	XP_011538341.1:p.Val745Gly
XM_011540040.1:c.2228T>G	XP_011538342.1:p.Val743Gly
XM_011540041.1:c.2174T>G	XP_011538343.1:p.Val725Gly
XM_011540042.1:c.2234T>G	XP_011538344.1:p.Val745Gly
XM_011540043.1:c.2234T>G	XP_011538345.1:p.Val745Gly
XM_011540044.1:c.2099T>G	XP_011538346.1:p.Val700Gly
XM_011540045.1:c.2234T>G	XP_011538347.1:p.Val745Gly
XM_011540046.1:c.1694T>G	XP_011538348.1:p.Val565Gly
XM_011540047.1:c.1052T>G	XP_011538349.1:p.Val351Gly
XM_011540048.1:c.2234T>G	XP_011538350.1:p.Val745Gly
XM_011540049.1:c.2234T>G	XP_011538351.1:p.Val745Gly
XM_011540050.1:c.2234T>G	XP_011538352.1:p.Val745Gly
XM_011540051.1:c.2234T>G	XP_011538353.1:p.Val745Gly
XM_011540053.1:c.2234T>G	XP_011538355.1:p.Val745Gly
XM_011540054.1:c.2174T>G	XP_011538356.1:p.Val725Gly
XR_945796.1:n.2477T>G
NM_001171930.2:c.2039T>G	NP_001165401.1:p.Val680Gly
NM_001171931.2:c.2039T>G	NP_001165402.1:p.Val680Gly
NM_022124.6:c.2039T>G MANE Select	NP_071407.4:p.Val680Gly