Canonical Allele Identifier: CA2609580403

Gene: CDH23

Linked Data

• gnomAD v4: 10-71793273-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793273C>T , CM000672.2:g.71793273C>T	GRCh38
NC_000010.10:g.73553030C>T , CM000672.1:g.73553030C>T	GRCh37
NC_000010.9:g.73223036C>T	NCBI36
NG_008835.1:g.401327C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6345C>T MANE Select	ENSP00000224721.9:p.Arg2115=
ENST00000224721.10:c.6360C>T	ENSP00000224721.8:p.Arg2120=
ENST00000622827.4:c.6345C>T	ENSP00000483211.1:p.Arg2115=
NM_022124.5:c.6345C>T	NP_071407.4:p.Arg2115=
XM_006717940.2:c.6540C>T	XP_006718003.1:p.Arg2180=
XM_006717942.2:c.6474C>T	XP_006718005.1:p.Arg2158=
XM_011540039.1:c.6537C>T	XP_011538341.1:p.Arg2179=
XM_011540040.1:c.6534C>T	XP_011538342.1:p.Arg2178=
XM_011540041.1:c.6480C>T	XP_011538343.1:p.Arg2160=
XM_011540042.1:c.6540C>T	XP_011538344.1:p.Arg2180=
XM_011540043.1:c.6540C>T	XP_011538345.1:p.Arg2180=
XM_011540044.1:c.6405C>T	XP_011538346.1:p.Arg2135=
XM_011540045.1:c.6540C>T	XP_011538347.1:p.Arg2180=
XM_011540046.1:c.6000C>T	XP_011538348.1:p.Arg2000=
XM_011540047.1:c.5358C>T	XP_011538349.1:p.Arg1786=
XM_011540048.1:c.6540C>T	XP_011538350.1:p.Arg2180=
XM_011540049.1:c.6540C>T	XP_011538351.1:p.Arg2180=
XM_011540050.1:c.6540C>T	XP_011538352.1:p.Arg2180=
XM_011540051.1:c.6540C>T	XP_011538353.1:p.Arg2180=
XM_011540052.1:c.2868C>T	XP_011538354.1:p.Arg956=
XR_945796.1:n.6783C>T
NM_022124.6:c.6345C>T MANE Select	NP_071407.4:p.Arg2115=