Canonical Allele Identifier: CA377147338

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73544853C>G (hg19) ; chr10:g.71785096C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71785096C>G , CM000672.2:g.71785096C>G	GRCh38
NC_000010.10:g.73544853C>G , CM000672.1:g.73544853C>G	GRCh37
NC_000010.9:g.73214859C>G	NCBI36
NG_008835.1:g.393150C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5708C>G MANE Select	ENSP00000224721.9:p.Ala1903Gly
ENST00000224721.10:c.5723C>G	ENSP00000224721.8:p.Ala1908Gly
ENST00000622827.4:c.5708C>G	ENSP00000483211.1:p.Ala1903Gly
NM_022124.5:c.5708C>G	NP_071407.4:p.Ala1903Gly
XM_006717940.2:c.5903C>G	XP_006718003.1:p.Ala1968Gly
XM_006717942.2:c.5837C>G	XP_006718005.1:p.Ala1946Gly
XM_011540039.1:c.5900C>G	XP_011538341.1:p.Ala1967Gly
XM_011540040.1:c.5897C>G	XP_011538342.1:p.Ala1966Gly
XM_011540041.1:c.5843C>G	XP_011538343.1:p.Ala1948Gly
XM_011540042.1:c.5903C>G	XP_011538344.1:p.Ala1968Gly
XM_011540043.1:c.5903C>G	XP_011538345.1:p.Ala1968Gly
XM_011540044.1:c.5768C>G	XP_011538346.1:p.Ala1923Gly
XM_011540045.1:c.5903C>G	XP_011538347.1:p.Ala1968Gly
XM_011540046.1:c.5363C>G	XP_011538348.1:p.Ala1788Gly
XM_011540047.1:c.4721C>G	XP_011538349.1:p.Ala1574Gly
XM_011540048.1:c.5903C>G	XP_011538350.1:p.Ala1968Gly
XM_011540049.1:c.5903C>G	XP_011538351.1:p.Ala1968Gly
XM_011540050.1:c.5903C>G	XP_011538352.1:p.Ala1968Gly
XM_011540051.1:c.5903C>G	XP_011538353.1:p.Ala1968Gly
XM_011540052.1:c.2231C>G	XP_011538354.1:p.Ala744Gly
XM_011540053.1:c.5903C>G	XP_011538355.1:p.Ala1968Gly
XR_945796.1:n.6146C>G
NM_022124.6:c.5708C>G MANE Select	NP_071407.4:p.Ala1903Gly