Canonical Allele Identifier: CA470053512

Gene: CDH23

Linked Data

• gnomAD v4: 10-71439840-C-G
• MyVariant Identifiers: chr10:g.73199597C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71439840C>G , CM000672.2:g.71439840C>G	GRCh38
NC_000010.10:g.73199597C>G , CM000672.1:g.73199597C>G	GRCh37
NC_000010.9:g.72869603C>G	NCBI36
NG_008835.1:g.47894C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.9C>G MANE Select	ENSP00000224721.9:p.Arg3=
ENST00000398809.9:c.9C>G	ENSP00000381789.5:p.Arg3=
ENST00000442677.4:c.9C>G	ENSP00000388894.3:p.Arg3=
ENST00000644511.1:c.130+42522C>G	ENSP00000495691.1:n.130+42522C>G
ENST00000224721.10:c.9C>G	ENSP00000224721.8:p.Arg3=
ENST00000299366.11:c.9C>G	ENSP00000299366.8:p.Arg3=
ENST00000398809.8:c.9C>G	ENSP00000381789.5:p.Arg3=
ENST00000398842.7:c.-33+42522C>G	ENSP00000381822.4:n.-33+42522C>G
ENST00000461841.7:c.9C>G	ENSP00000473454.2:p.Arg3=
ENST00000616684.4:c.9C>G	ENSP00000482036.2:p.Arg3=
ENST00000622827.4:c.9C>G	ENSP00000483211.1:p.Arg3=
NM_001171930.1:c.9C>G	NP_001165401.1:p.Arg3=
NM_001171931.1:c.9C>G	NP_001165402.1:p.Arg3=
NM_001171932.1:c.9C>G	NP_001165403.1:p.Arg3=
NM_022124.5:c.9C>G	NP_071407.4:p.Arg3=
NM_052836.3:c.9C>G	NP_443068.1:p.Arg3=
XM_006717940.2:c.144C>G	XP_006718003.1:p.Arg48=
XM_006717942.2:c.144C>G	XP_006718005.1:p.Arg48=
XM_011540039.1:c.144C>G	XP_011538341.1:p.Arg48=
XM_011540040.1:c.144C>G	XP_011538342.1:p.Arg48=
XM_011540041.1:c.144C>G	XP_011538343.1:p.Arg48=
XM_011540042.1:c.144C>G	XP_011538344.1:p.Arg48=
XM_011540043.1:c.144C>G	XP_011538345.1:p.Arg48=
XM_011540044.1:c.9C>G	XP_011538346.1:p.Arg3=
XM_011540045.1:c.144C>G	XP_011538347.1:p.Arg48=
XM_011540048.1:c.144C>G	XP_011538350.1:p.Arg48=
XM_011540049.1:c.144C>G	XP_011538351.1:p.Arg48=
XM_011540050.1:c.144C>G	XP_011538352.1:p.Arg48=
XM_011540051.1:c.144C>G	XP_011538353.1:p.Arg48=
XM_011540053.1:c.144C>G	XP_011538355.1:p.Arg48=
XM_011540054.1:c.144C>G	XP_011538356.1:p.Arg48=
XR_945796.1:n.387C>G
NM_001171930.2:c.9C>G	NP_001165401.1:p.Arg3=
NM_001171931.2:c.9C>G	NP_001165402.1:p.Arg3=
NM_022124.6:c.9C>G MANE Select	NP_071407.4:p.Arg3=
NM_052836.4:c.9C>G	NP_443068.1:p.Arg3=
NM_001171932.2:c.9C>G	NP_001165403.1:p.Arg3=