Canonical Allele Identifier: CA209466076

Gene: CDH23

Linked Data

• dbSNP Id: rs946465505
• MyVariant Identifiers: chr10:g.73553096G>T (hg19) ; chr10:g.71793339G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793339G>T , CM000672.2:g.71793339G>T	GRCh38
NC_000010.10:g.73553096G>T , CM000672.1:g.73553096G>T	GRCh37
NC_000010.9:g.73223102G>T	NCBI36
NG_008835.1:g.401393G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6411G>T MANE Select	ENSP00000224721.9:p.Gln2137His
ENST00000224721.10:c.6426G>T	ENSP00000224721.8:p.Gln2142His
ENST00000622827.4:c.6411G>T	ENSP00000483211.1:p.Gln2137His
NM_022124.5:c.6411G>T	NP_071407.4:p.Gln2137His
XM_006717940.2:c.6606G>T	XP_006718003.1:p.Gln2202His
XM_006717942.2:c.6540G>T	XP_006718005.1:p.Gln2180His
XM_011540039.1:c.6603G>T	XP_011538341.1:p.Gln2201His
XM_011540040.1:c.6600G>T	XP_011538342.1:p.Gln2200His
XM_011540041.1:c.6546G>T	XP_011538343.1:p.Gln2182His
XM_011540042.1:c.6577+29G>T	XP_011538344.1:n.6577+29G>T
XM_011540043.1:c.6606G>T	XP_011538345.1:p.Gln2202His
XM_011540044.1:c.6471G>T	XP_011538346.1:p.Gln2157His
XM_011540045.1:c.6606G>T	XP_011538347.1:p.Gln2202His
XM_011540046.1:c.6066G>T	XP_011538348.1:p.Gln2022His
XM_011540047.1:c.5424G>T	XP_011538349.1:p.Gln1808His
XM_011540048.1:c.6606G>T	XP_011538350.1:p.Gln2202His
XM_011540049.1:c.6606G>T	XP_011538351.1:p.Gln2202His
XM_011540050.1:c.6606G>T	XP_011538352.1:p.Gln2202His
XM_011540051.1:c.6606G>T	XP_011538353.1:p.Gln2202His
XM_011540052.1:c.2934G>T	XP_011538354.1:p.Gln978His
XR_945796.1:n.6849G>T
NM_022124.6:c.6411G>T MANE Select	NP_071407.4:p.Gln2137His