Canonical Allele Identifier: CA377160756
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71740932C>G , CM000672.2:g.71740932C>G GRCh38
NC_000010.10:g.73500689C>G , CM000672.1:g.73500689C>G GRCh37
NC_000010.9:g.73170695C>G NCBI36
NG_008835.1:g.348986C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.4599C>G MANE Select ENSP00000224721.9:p.Tyr1533Ter
ENST00000224721.10:c.4614C>G ENSP00000224721.8:p.Tyr1538Ter
ENST00000398792.3:n.1288C>G
ENST00000622827.4:c.4599C>G ENSP00000483211.1:p.Tyr1533Ter
NM_022124.5:c.4599C>G NP_071407.4:p.Tyr1533Ter
XM_006717940.2:c.4794C>G XP_006718003.1:p.Tyr1598Ter
XM_006717942.2:c.4728C>G XP_006718005.1:p.Tyr1576Ter
XM_011540039.1:c.4791C>G XP_011538341.1:p.Tyr1597Ter
XM_011540040.1:c.4788C>G XP_011538342.1:p.Tyr1596Ter
XM_011540041.1:c.4734C>G XP_011538343.1:p.Tyr1578Ter
XM_011540042.1:c.4794C>G XP_011538344.1:p.Tyr1598Ter
XM_011540043.1:c.4794C>G XP_011538345.1:p.Tyr1598Ter
XM_011540044.1:c.4659C>G XP_011538346.1:p.Tyr1553Ter
XM_011540045.1:c.4794C>G XP_011538347.1:p.Tyr1598Ter
XM_011540046.1:c.4254C>G XP_011538348.1:p.Tyr1418Ter
XM_011540047.1:c.3612C>G XP_011538349.1:p.Tyr1204Ter
XM_011540048.1:c.4794C>G XP_011538350.1:p.Tyr1598Ter
XM_011540049.1:c.4794C>G XP_011538351.1:p.Tyr1598Ter
XM_011540050.1:c.4794C>G XP_011538352.1:p.Tyr1598Ter
XM_011540051.1:c.4794C>G XP_011538353.1:p.Tyr1598Ter
XM_011540052.1:c.1122C>G XP_011538354.1:p.Tyr374Ter
XM_011540053.1:c.4794C>G XP_011538355.1:p.Tyr1598Ter
XR_945796.1:n.5037C>G
NM_022124.6:c.4599C>G MANE Select NP_071407.4:p.Tyr1533Ter