Canonical Allele Identifier: CA377154802

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73553086G>C (hg19) ; chr10:g.71793329G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793329G>C , CM000672.2:g.71793329G>C	GRCh38
NC_000010.10:g.73553086G>C , CM000672.1:g.73553086G>C	GRCh37
NC_000010.9:g.73223092G>C	NCBI36
NG_008835.1:g.401383G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6401G>C MANE Select	ENSP00000224721.9:p.Arg2134Thr
ENST00000224721.10:c.6416G>C	ENSP00000224721.8:p.Arg2139Thr
ENST00000622827.4:c.6401G>C	ENSP00000483211.1:p.Arg2134Thr
NM_022124.5:c.6401G>C	NP_071407.4:p.Arg2134Thr
XM_006717940.2:c.6596G>C	XP_006718003.1:p.Arg2199Thr
XM_006717942.2:c.6530G>C	XP_006718005.1:p.Arg2177Thr
XM_011540039.1:c.6593G>C	XP_011538341.1:p.Arg2198Thr
XM_011540040.1:c.6590G>C	XP_011538342.1:p.Arg2197Thr
XM_011540041.1:c.6536G>C	XP_011538343.1:p.Arg2179Thr
XM_011540042.1:c.6577+19G>C	XP_011538344.1:n.6577+19G>C
XM_011540043.1:c.6596G>C	XP_011538345.1:p.Arg2199Thr
XM_011540044.1:c.6461G>C	XP_011538346.1:p.Arg2154Thr
XM_011540045.1:c.6596G>C	XP_011538347.1:p.Arg2199Thr
XM_011540046.1:c.6056G>C	XP_011538348.1:p.Arg2019Thr
XM_011540047.1:c.5414G>C	XP_011538349.1:p.Arg1805Thr
XM_011540048.1:c.6596G>C	XP_011538350.1:p.Arg2199Thr
XM_011540049.1:c.6596G>C	XP_011538351.1:p.Arg2199Thr
XM_011540050.1:c.6596G>C	XP_011538352.1:p.Arg2199Thr
XM_011540051.1:c.6596G>C	XP_011538353.1:p.Arg2199Thr
XM_011540052.1:c.2924G>C	XP_011538354.1:p.Arg975Thr
XR_945796.1:n.6839G>C
NM_022124.6:c.6401G>C MANE Select	NP_071407.4:p.Arg2134Thr