Canonical Allele Identifier: CA377143292
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71709158T>G , CM000672.2:g.71709158T>G GRCh38
NC_000010.10:g.73468915T>G , CM000672.1:g.73468915T>G GRCh37
NC_000010.9:g.73138921T>G NCBI36
NG_008835.1:g.317212T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.3167T>G MANE Select ENSP00000224721.9:p.Val1056Gly
ENST00000398809.9:c.3167T>G ENSP00000381789.5:p.Val1056Gly
ENST00000442677.4:c.3167T>G ENSP00000388894.3:p.Val1056Gly
ENST00000466757.8:c.2598T>G
ENST00000224721.10:c.3182T>G ENSP00000224721.8:p.Val1061Gly
ENST00000398809.8:c.3167T>G ENSP00000381789.5:p.Val1056Gly
ENST00000442677.3:c.1942T>G
ENST00000466757.7:c.2598T>G
ENST00000616684.4:c.3167T>G ENSP00000482036.2:p.Val1056Gly
ENST00000622827.4:c.3167T>G ENSP00000483211.1:p.Val1056Gly
NM_001171930.1:c.3167T>G NP_001165401.1:p.Val1056Gly
NM_022124.5:c.3167T>G NP_071407.4:p.Val1056Gly
XM_006717940.2:c.3362T>G XP_006718003.1:p.Val1121Gly
XM_006717942.2:c.3296T>G XP_006718005.1:p.Val1099Gly
XM_011540039.1:c.3362T>G XP_011538341.1:p.Val1121Gly
XM_011540040.1:c.3356T>G XP_011538342.1:p.Val1119Gly
XM_011540041.1:c.3302T>G XP_011538343.1:p.Val1101Gly
XM_011540042.1:c.3362T>G XP_011538344.1:p.Val1121Gly
XM_011540043.1:c.3362T>G XP_011538345.1:p.Val1121Gly
XM_011540044.1:c.3227T>G XP_011538346.1:p.Val1076Gly
XM_011540045.1:c.3362T>G XP_011538347.1:p.Val1121Gly
XM_011540046.1:c.2822T>G XP_011538348.1:p.Val941Gly
XM_011540047.1:c.2180T>G XP_011538349.1:p.Val727Gly
XM_011540048.1:c.3362T>G XP_011538350.1:p.Val1121Gly
XM_011540049.1:c.3362T>G XP_011538351.1:p.Val1121Gly
XM_011540050.1:c.3362T>G XP_011538352.1:p.Val1121Gly
XM_011540051.1:c.3362T>G XP_011538353.1:p.Val1121Gly
XM_011540053.1:c.3362T>G XP_011538355.1:p.Val1121Gly
XR_945796.1:n.3605T>G
NM_001171930.2:c.3167T>G NP_001165401.1:p.Val1056Gly
NM_022124.6:c.3167T>G MANE Select NP_071407.4:p.Val1056Gly