Canonical Allele Identifier: CA2609580476
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71793321C>G , CM000672.2:g.71793321C>G GRCh38
NC_000010.10:g.73553078C>G , CM000672.1:g.73553078C>G GRCh37
NC_000010.9:g.73223084C>G NCBI36
NG_008835.1:g.401375C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.6393C>G MANE Select ENSP00000224721.9:p.Thr2131=
ENST00000224721.10:c.6408C>G ENSP00000224721.8:p.Thr2136=
ENST00000622827.4:c.6393C>G ENSP00000483211.1:p.Thr2131=
NM_022124.5:c.6393C>G NP_071407.4:p.Thr2131=
XM_006717940.2:c.6588C>G XP_006718003.1:p.Thr2196=
XM_006717942.2:c.6522C>G XP_006718005.1:p.Thr2174=
XM_011540039.1:c.6585C>G XP_011538341.1:p.Thr2195=
XM_011540040.1:c.6582C>G XP_011538342.1:p.Thr2194=
XM_011540041.1:c.6528C>G XP_011538343.1:p.Thr2176=
XM_011540042.1:c.6577+11C>G XP_011538344.1:n.6577+11C>G
XM_011540043.1:c.6588C>G XP_011538345.1:p.Thr2196=
XM_011540044.1:c.6453C>G XP_011538346.1:p.Thr2151=
XM_011540045.1:c.6588C>G XP_011538347.1:p.Thr2196=
XM_011540046.1:c.6048C>G XP_011538348.1:p.Thr2016=
XM_011540047.1:c.5406C>G XP_011538349.1:p.Thr1802=
XM_011540048.1:c.6588C>G XP_011538350.1:p.Thr2196=
XM_011540049.1:c.6588C>G XP_011538351.1:p.Thr2196=
XM_011540050.1:c.6588C>G XP_011538352.1:p.Thr2196=
XM_011540051.1:c.6588C>G XP_011538353.1:p.Thr2196=
XM_011540052.1:c.2916C>G XP_011538354.1:p.Thr972=
XR_945796.1:n.6831C>G
NM_022124.6:c.6393C>G MANE Select NP_071407.4:p.Thr2131=