Canonical Allele Identifier: CA470060775

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73544800C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71785043C>G , CM000672.2:g.71785043C>G	GRCh38
NC_000010.10:g.73544800C>G , CM000672.1:g.73544800C>G	GRCh37
NC_000010.9:g.73214806C>G	NCBI36
NG_008835.1:g.393097C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5655C>G MANE Select	ENSP00000224721.9:p.Arg1885=
ENST00000224721.10:c.5670C>G	ENSP00000224721.8:p.Arg1890=
ENST00000622827.4:c.5655C>G	ENSP00000483211.1:p.Arg1885=
NM_022124.5:c.5655C>G	NP_071407.4:p.Arg1885=
XM_006717940.2:c.5850C>G	XP_006718003.1:p.Arg1950=
XM_006717942.2:c.5784C>G	XP_006718005.1:p.Arg1928=
XM_011540039.1:c.5847C>G	XP_011538341.1:p.Arg1949=
XM_011540040.1:c.5844C>G	XP_011538342.1:p.Arg1948=
XM_011540041.1:c.5790C>G	XP_011538343.1:p.Arg1930=
XM_011540042.1:c.5850C>G	XP_011538344.1:p.Arg1950=
XM_011540043.1:c.5850C>G	XP_011538345.1:p.Arg1950=
XM_011540044.1:c.5715C>G	XP_011538346.1:p.Arg1905=
XM_011540045.1:c.5850C>G	XP_011538347.1:p.Arg1950=
XM_011540046.1:c.5310C>G	XP_011538348.1:p.Arg1770=
XM_011540047.1:c.4668C>G	XP_011538349.1:p.Arg1556=
XM_011540048.1:c.5850C>G	XP_011538350.1:p.Arg1950=
XM_011540049.1:c.5850C>G	XP_011538351.1:p.Arg1950=
XM_011540050.1:c.5850C>G	XP_011538352.1:p.Arg1950=
XM_011540051.1:c.5850C>G	XP_011538353.1:p.Arg1950=
XM_011540052.1:c.2178C>G	XP_011538354.1:p.Arg726=
XM_011540053.1:c.5850C>G	XP_011538355.1:p.Arg1950=
XR_945796.1:n.6093C>G
NM_022124.6:c.5655C>G MANE Select	NP_071407.4:p.Arg1885=