Canonical Allele Identifier: CA377147091

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73544822G>C (hg19) ; chr10:g.71785065G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71785065G>C , CM000672.2:g.71785065G>C	GRCh38
NC_000010.10:g.73544822G>C , CM000672.1:g.73544822G>C	GRCh37
NC_000010.9:g.73214828G>C	NCBI36
NG_008835.1:g.393119G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5677G>C MANE Select	ENSP00000224721.9:p.Gly1893Arg
ENST00000224721.10:c.5692G>C	ENSP00000224721.8:p.Gly1898Arg
ENST00000622827.4:c.5677G>C	ENSP00000483211.1:p.Gly1893Arg
NM_022124.5:c.5677G>C	NP_071407.4:p.Gly1893Arg
XM_006717940.2:c.5872G>C	XP_006718003.1:p.Gly1958Arg
XM_006717942.2:c.5806G>C	XP_006718005.1:p.Gly1936Arg
XM_011540039.1:c.5869G>C	XP_011538341.1:p.Gly1957Arg
XM_011540040.1:c.5866G>C	XP_011538342.1:p.Gly1956Arg
XM_011540041.1:c.5812G>C	XP_011538343.1:p.Gly1938Arg
XM_011540042.1:c.5872G>C	XP_011538344.1:p.Gly1958Arg
XM_011540043.1:c.5872G>C	XP_011538345.1:p.Gly1958Arg
XM_011540044.1:c.5737G>C	XP_011538346.1:p.Gly1913Arg
XM_011540045.1:c.5872G>C	XP_011538347.1:p.Gly1958Arg
XM_011540046.1:c.5332G>C	XP_011538348.1:p.Gly1778Arg
XM_011540047.1:c.4690G>C	XP_011538349.1:p.Gly1564Arg
XM_011540048.1:c.5872G>C	XP_011538350.1:p.Gly1958Arg
XM_011540049.1:c.5872G>C	XP_011538351.1:p.Gly1958Arg
XM_011540050.1:c.5872G>C	XP_011538352.1:p.Gly1958Arg
XM_011540051.1:c.5872G>C	XP_011538353.1:p.Gly1958Arg
XM_011540052.1:c.2200G>C	XP_011538354.1:p.Gly734Arg
XM_011540053.1:c.5872G>C	XP_011538355.1:p.Gly1958Arg
XR_945796.1:n.6115G>C
NM_022124.6:c.5677G>C MANE Select	NP_071407.4:p.Gly1893Arg