Canonical Allele Identifier: CA377155336
Gene: CDH23 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71793500C>G , CM000672.2:g.71793500C>G GRCh38
NC_000010.10:g.73553257C>G , CM000672.1:g.73553257C>G GRCh37
NC_000010.9:g.73223263C>G NCBI36
NG_008835.1:g.401554C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.6572C>G MANE Select ENSP00000224721.9:p.Thr2191Ser
ENST00000224721.10:c.6587C>G ENSP00000224721.8:p.Thr2196Ser
ENST00000622827.4:c.6572C>G ENSP00000483211.1:p.Thr2191Ser
NM_022124.5:c.6572C>G NP_071407.4:p.Thr2191Ser
XM_006717940.2:c.6767C>G XP_006718003.1:p.Thr2256Ser
XM_006717942.2:c.6701C>G XP_006718005.1:p.Thr2234Ser
XM_011540039.1:c.6764C>G XP_011538341.1:p.Thr2255Ser
XM_011540040.1:c.6761C>G XP_011538342.1:p.Thr2254Ser
XM_011540041.1:c.6707C>G XP_011538343.1:p.Thr2236Ser
XM_011540042.1:c.6677C>G XP_011538344.1:p.Thr2226Ser
XM_011540043.1:c.6767C>G XP_011538345.1:p.Thr2256Ser
XM_011540044.1:c.6632C>G XP_011538346.1:p.Thr2211Ser
XM_011540045.1:c.6767C>G XP_011538347.1:p.Thr2256Ser
XM_011540046.1:c.6227C>G XP_011538348.1:p.Thr2076Ser
XM_011540047.1:c.5585C>G XP_011538349.1:p.Thr1862Ser
XM_011540048.1:c.6767C>G XP_011538350.1:p.Thr2256Ser
XM_011540049.1:c.6767C>G XP_011538351.1:p.Thr2256Ser
XM_011540050.1:c.6767C>G XP_011538352.1:p.Thr2256Ser
XM_011540051.1:c.6767C>G XP_011538353.1:p.Thr2256Ser
XM_011540052.1:c.3095C>G XP_011538354.1:p.Thr1032Ser
XR_945796.1:n.7010C>G
NM_022124.6:c.6572C>G MANE Select NP_071407.4:p.Thr2191Ser
Search 100 bp 5'
Search 100 bp 3'