Canonical Allele Identifier: CA470058016

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73405704G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71645947G>A , CM000672.2:g.71645947G>A	GRCh38
NC_000010.10:g.73405704G>A , CM000672.1:g.73405704G>A	GRCh37
NC_000010.9:g.73075710G>A	NCBI36
NG_008835.1:g.254001G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.1257G>A MANE Select	ENSP00000224721.9:p.Leu419=
ENST00000398809.9:c.1257G>A	ENSP00000381789.5:p.Leu419=
ENST00000442677.4:c.1257G>A	ENSP00000388894.3:p.Leu419=
ENST00000466757.8:c.688G>A
ENST00000643732.1:n.1093G>A
ENST00000646131.1:c.921G>A	ENSP00000495098.1:p.Leu307=
ENST00000224721.10:c.1272G>A	ENSP00000224721.8:p.Leu424=
ENST00000299366.11:c.1257G>A	ENSP00000299366.8:p.Leu419=
ENST00000398809.8:c.1257G>A	ENSP00000381789.5:p.Leu419=
ENST00000398842.7:c.1002G>A	ENSP00000381822.4:p.Leu334=
ENST00000442677.3:c.32G>A
ENST00000461841.7:c.1257G>A	ENSP00000473454.2:p.Leu419=
ENST00000466757.7:c.688G>A
ENST00000470494.5:c.226G>A
ENST00000616684.4:c.1257G>A	ENSP00000482036.2:p.Leu419=
ENST00000622827.4:c.1257G>A	ENSP00000483211.1:p.Leu419=
NM_001171930.1:c.1257G>A	NP_001165401.1:p.Leu419=
NM_001171931.1:c.1257G>A	NP_001165402.1:p.Leu419=
NM_022124.5:c.1257G>A	NP_071407.4:p.Leu419=
NM_052836.3:c.1257G>A	NP_443068.1:p.Leu419=
XM_006717940.2:c.1452G>A	XP_006718003.1:p.Leu484=
XM_006717942.2:c.1386G>A	XP_006718005.1:p.Leu462=
XM_011540039.1:c.1452G>A	XP_011538341.1:p.Leu484=
XM_011540040.1:c.1446G>A	XP_011538342.1:p.Leu482=
XM_011540041.1:c.1392G>A	XP_011538343.1:p.Leu464=
XM_011540042.1:c.1452G>A	XP_011538344.1:p.Leu484=
XM_011540043.1:c.1452G>A	XP_011538345.1:p.Leu484=
XM_011540044.1:c.1317G>A	XP_011538346.1:p.Leu439=
XM_011540045.1:c.1452G>A	XP_011538347.1:p.Leu484=
XM_011540046.1:c.912G>A	XP_011538348.1:p.Leu304=
XM_011540047.1:c.270G>A	XP_011538349.1:p.Leu90=
XM_011540048.1:c.1452G>A	XP_011538350.1:p.Leu484=
XM_011540049.1:c.1452G>A	XP_011538351.1:p.Leu484=
XM_011540050.1:c.1452G>A	XP_011538352.1:p.Leu484=
XM_011540051.1:c.1452G>A	XP_011538353.1:p.Leu484=
XM_011540053.1:c.1452G>A	XP_011538355.1:p.Leu484=
XM_011540054.1:c.1392G>A	XP_011538356.1:p.Leu464=
XR_945796.1:n.1695G>A
NM_001171930.2:c.1257G>A	NP_001165401.1:p.Leu419=
NM_001171931.2:c.1257G>A	NP_001165402.1:p.Leu419=
NM_022124.6:c.1257G>A MANE Select	NP_071407.4:p.Leu419=
NM_052836.4:c.1257G>A	NP_443068.1:p.Leu419=