Canonical Allele Identifier: CA377146672

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73544731G>C (hg19) ; chr10:g.71784974G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71784974G>C , CM000672.2:g.71784974G>C	GRCh38
NC_000010.10:g.73544731G>C , CM000672.1:g.73544731G>C	GRCh37
NC_000010.9:g.73214737G>C	NCBI36
NG_008835.1:g.393028G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5586G>C MANE Select	ENSP00000224721.9:p.Glu1862Asp
ENST00000224721.10:c.5601G>C	ENSP00000224721.8:p.Glu1867Asp
ENST00000622827.4:c.5586G>C	ENSP00000483211.1:p.Glu1862Asp
NM_022124.5:c.5586G>C	NP_071407.4:p.Glu1862Asp
XM_006717940.2:c.5781G>C	XP_006718003.1:p.Glu1927Asp
XM_006717942.2:c.5715G>C	XP_006718005.1:p.Glu1905Asp
XM_011540039.1:c.5778G>C	XP_011538341.1:p.Glu1926Asp
XM_011540040.1:c.5775G>C	XP_011538342.1:p.Glu1925Asp
XM_011540041.1:c.5721G>C	XP_011538343.1:p.Glu1907Asp
XM_011540042.1:c.5781G>C	XP_011538344.1:p.Glu1927Asp
XM_011540043.1:c.5781G>C	XP_011538345.1:p.Glu1927Asp
XM_011540044.1:c.5646G>C	XP_011538346.1:p.Glu1882Asp
XM_011540045.1:c.5781G>C	XP_011538347.1:p.Glu1927Asp
XM_011540046.1:c.5241G>C	XP_011538348.1:p.Glu1747Asp
XM_011540047.1:c.4599G>C	XP_011538349.1:p.Glu1533Asp
XM_011540048.1:c.5781G>C	XP_011538350.1:p.Glu1927Asp
XM_011540049.1:c.5781G>C	XP_011538351.1:p.Glu1927Asp
XM_011540050.1:c.5781G>C	XP_011538352.1:p.Glu1927Asp
XM_011540051.1:c.5781G>C	XP_011538353.1:p.Glu1927Asp
XM_011540052.1:c.2109G>C	XP_011538354.1:p.Glu703Asp
XM_011540053.1:c.5781G>C	XP_011538355.1:p.Glu1927Asp
XR_945796.1:n.6024G>C
NM_022124.6:c.5586G>C MANE Select	NP_071407.4:p.Glu1862Asp