Canonical Allele Identifier: CA377160323
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71740831T>G , CM000672.2:g.71740831T>G GRCh38
NC_000010.10:g.73500588T>G , CM000672.1:g.73500588T>G GRCh37
NC_000010.9:g.73170594T>G NCBI36
NG_008835.1:g.348885T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.4498T>G MANE Select ENSP00000224721.9:p.Ser1500Ala
ENST00000224721.10:c.4513T>G ENSP00000224721.8:p.Ser1505Ala
ENST00000398792.3:n.1187T>G
ENST00000622827.4:c.4498T>G ENSP00000483211.1:p.Ser1500Ala
NM_022124.5:c.4498T>G NP_071407.4:p.Ser1500Ala
XM_006717940.2:c.4693T>G XP_006718003.1:p.Ser1565Ala
XM_006717942.2:c.4627T>G XP_006718005.1:p.Ser1543Ala
XM_011540039.1:c.4690T>G XP_011538341.1:p.Ser1564Ala
XM_011540040.1:c.4687T>G XP_011538342.1:p.Ser1563Ala
XM_011540041.1:c.4633T>G XP_011538343.1:p.Ser1545Ala
XM_011540042.1:c.4693T>G XP_011538344.1:p.Ser1565Ala
XM_011540043.1:c.4693T>G XP_011538345.1:p.Ser1565Ala
XM_011540044.1:c.4558T>G XP_011538346.1:p.Ser1520Ala
XM_011540045.1:c.4693T>G XP_011538347.1:p.Ser1565Ala
XM_011540046.1:c.4153T>G XP_011538348.1:p.Ser1385Ala
XM_011540047.1:c.3511T>G XP_011538349.1:p.Ser1171Ala
XM_011540048.1:c.4693T>G XP_011538350.1:p.Ser1565Ala
XM_011540049.1:c.4693T>G XP_011538351.1:p.Ser1565Ala
XM_011540050.1:c.4693T>G XP_011538352.1:p.Ser1565Ala
XM_011540051.1:c.4693T>G XP_011538353.1:p.Ser1565Ala
XM_011540052.1:c.1021T>G XP_011538354.1:p.Ser341Ala
XM_011540053.1:c.4693T>G XP_011538355.1:p.Ser1565Ala
XR_945796.1:n.4936T>G
NM_022124.6:c.4498T>G MANE Select NP_071407.4:p.Ser1500Ala