Canonical Allele Identifier: CA377154758

Gene: CDH23

Linked Data

• dbSNP Id: rs896709276
• MyVariant Identifiers: chr10:g.73553082G>C (hg19) ; chr10:g.71793325G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793325G>C , CM000672.2:g.71793325G>C	GRCh38
NC_000010.10:g.73553082G>C , CM000672.1:g.73553082G>C	GRCh37
NC_000010.9:g.73223088G>C	NCBI36
NG_008835.1:g.401379G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6397G>C MANE Select	ENSP00000224721.9:p.Asp2133His
ENST00000224721.10:c.6412G>C	ENSP00000224721.8:p.Asp2138His
ENST00000622827.4:c.6397G>C	ENSP00000483211.1:p.Asp2133His
NM_022124.5:c.6397G>C	NP_071407.4:p.Asp2133His
XM_006717940.2:c.6592G>C	XP_006718003.1:p.Asp2198His
XM_006717942.2:c.6526G>C	XP_006718005.1:p.Asp2176His
XM_011540039.1:c.6589G>C	XP_011538341.1:p.Asp2197His
XM_011540040.1:c.6586G>C	XP_011538342.1:p.Asp2196His
XM_011540041.1:c.6532G>C	XP_011538343.1:p.Asp2178His
XM_011540042.1:c.6577+15G>C	XP_011538344.1:n.6577+15G>C
XM_011540043.1:c.6592G>C	XP_011538345.1:p.Asp2198His
XM_011540044.1:c.6457G>C	XP_011538346.1:p.Asp2153His
XM_011540045.1:c.6592G>C	XP_011538347.1:p.Asp2198His
XM_011540046.1:c.6052G>C	XP_011538348.1:p.Asp2018His
XM_011540047.1:c.5410G>C	XP_011538349.1:p.Asp1804His
XM_011540048.1:c.6592G>C	XP_011538350.1:p.Asp2198His
XM_011540049.1:c.6592G>C	XP_011538351.1:p.Asp2198His
XM_011540050.1:c.6592G>C	XP_011538352.1:p.Asp2198His
XM_011540051.1:c.6592G>C	XP_011538353.1:p.Asp2198His
XM_011540052.1:c.2920G>C	XP_011538354.1:p.Asp974His
XR_945796.1:n.6835G>C
NM_022124.6:c.6397G>C MANE Select	NP_071407.4:p.Asp2133His