Canonical Allele Identifier: CA470060743

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73544746C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71784989C>G , CM000672.2:g.71784989C>G	GRCh38
NC_000010.10:g.73544746C>G , CM000672.1:g.73544746C>G	GRCh37
NC_000010.9:g.73214752C>G	NCBI36
NG_008835.1:g.393043C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5601C>G MANE Select	ENSP00000224721.9:p.Ser1867=
ENST00000224721.10:c.5616C>G	ENSP00000224721.8:p.Ser1872=
ENST00000622827.4:c.5601C>G	ENSP00000483211.1:p.Ser1867=
NM_022124.5:c.5601C>G	NP_071407.4:p.Ser1867=
XM_006717940.2:c.5796C>G	XP_006718003.1:p.Ser1932=
XM_006717942.2:c.5730C>G	XP_006718005.1:p.Ser1910=
XM_011540039.1:c.5793C>G	XP_011538341.1:p.Ser1931=
XM_011540040.1:c.5790C>G	XP_011538342.1:p.Ser1930=
XM_011540041.1:c.5736C>G	XP_011538343.1:p.Ser1912=
XM_011540042.1:c.5796C>G	XP_011538344.1:p.Ser1932=
XM_011540043.1:c.5796C>G	XP_011538345.1:p.Ser1932=
XM_011540044.1:c.5661C>G	XP_011538346.1:p.Ser1887=
XM_011540045.1:c.5796C>G	XP_011538347.1:p.Ser1932=
XM_011540046.1:c.5256C>G	XP_011538348.1:p.Ser1752=
XM_011540047.1:c.4614C>G	XP_011538349.1:p.Ser1538=
XM_011540048.1:c.5796C>G	XP_011538350.1:p.Ser1932=
XM_011540049.1:c.5796C>G	XP_011538351.1:p.Ser1932=
XM_011540050.1:c.5796C>G	XP_011538352.1:p.Ser1932=
XM_011540051.1:c.5796C>G	XP_011538353.1:p.Ser1932=
XM_011540052.1:c.2124C>G	XP_011538354.1:p.Ser708=
XM_011540053.1:c.5796C>G	XP_011538355.1:p.Ser1932=
XR_945796.1:n.6039C>G
NM_022124.6:c.5601C>G MANE Select	NP_071407.4:p.Ser1867=