Canonical Allele Identifier: CA377147083

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73544819G>C (hg19) ; chr10:g.71785062G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71785062G>C , CM000672.2:g.71785062G>C	GRCh38
NC_000010.10:g.73544819G>C , CM000672.1:g.73544819G>C	GRCh37
NC_000010.9:g.73214825G>C	NCBI36
NG_008835.1:g.393116G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5674G>C MANE Select	ENSP00000224721.9:p.Ala1892Pro
ENST00000224721.10:c.5689G>C	ENSP00000224721.8:p.Ala1897Pro
ENST00000622827.4:c.5674G>C	ENSP00000483211.1:p.Ala1892Pro
NM_022124.5:c.5674G>C	NP_071407.4:p.Ala1892Pro
XM_006717940.2:c.5869G>C	XP_006718003.1:p.Ala1957Pro
XM_006717942.2:c.5803G>C	XP_006718005.1:p.Ala1935Pro
XM_011540039.1:c.5866G>C	XP_011538341.1:p.Ala1956Pro
XM_011540040.1:c.5863G>C	XP_011538342.1:p.Ala1955Pro
XM_011540041.1:c.5809G>C	XP_011538343.1:p.Ala1937Pro
XM_011540042.1:c.5869G>C	XP_011538344.1:p.Ala1957Pro
XM_011540043.1:c.5869G>C	XP_011538345.1:p.Ala1957Pro
XM_011540044.1:c.5734G>C	XP_011538346.1:p.Ala1912Pro
XM_011540045.1:c.5869G>C	XP_011538347.1:p.Ala1957Pro
XM_011540046.1:c.5329G>C	XP_011538348.1:p.Ala1777Pro
XM_011540047.1:c.4687G>C	XP_011538349.1:p.Ala1563Pro
XM_011540048.1:c.5869G>C	XP_011538350.1:p.Ala1957Pro
XM_011540049.1:c.5869G>C	XP_011538351.1:p.Ala1957Pro
XM_011540050.1:c.5869G>C	XP_011538352.1:p.Ala1957Pro
XM_011540051.1:c.5869G>C	XP_011538353.1:p.Ala1957Pro
XM_011540052.1:c.2197G>C	XP_011538354.1:p.Ala733Pro
XM_011540053.1:c.5869G>C	XP_011538355.1:p.Ala1957Pro
XR_945796.1:n.6112G>C
NM_022124.6:c.5674G>C MANE Select	NP_071407.4:p.Ala1892Pro