Canonical Allele Identifier: CA377160481
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71740870C>A , CM000672.2:g.71740870C>A GRCh38
NC_000010.10:g.73500627C>A , CM000672.1:g.73500627C>A GRCh37
NC_000010.9:g.73170633C>A NCBI36
NG_008835.1:g.348924C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.4537C>A MANE Select ENSP00000224721.9:p.Leu1513Met
ENST00000224721.10:c.4552C>A ENSP00000224721.8:p.Leu1518Met
ENST00000398792.3:n.1226C>A
ENST00000622827.4:c.4537C>A ENSP00000483211.1:p.Leu1513Met
NM_022124.5:c.4537C>A NP_071407.4:p.Leu1513Met
XM_006717940.2:c.4732C>A XP_006718003.1:p.Leu1578Met
XM_006717942.2:c.4666C>A XP_006718005.1:p.Leu1556Met
XM_011540039.1:c.4729C>A XP_011538341.1:p.Leu1577Met
XM_011540040.1:c.4726C>A XP_011538342.1:p.Leu1576Met
XM_011540041.1:c.4672C>A XP_011538343.1:p.Leu1558Met
XM_011540042.1:c.4732C>A XP_011538344.1:p.Leu1578Met
XM_011540043.1:c.4732C>A XP_011538345.1:p.Leu1578Met
XM_011540044.1:c.4597C>A XP_011538346.1:p.Leu1533Met
XM_011540045.1:c.4732C>A XP_011538347.1:p.Leu1578Met
XM_011540046.1:c.4192C>A XP_011538348.1:p.Leu1398Met
XM_011540047.1:c.3550C>A XP_011538349.1:p.Leu1184Met
XM_011540048.1:c.4732C>A XP_011538350.1:p.Leu1578Met
XM_011540049.1:c.4732C>A XP_011538351.1:p.Leu1578Met
XM_011540050.1:c.4732C>A XP_011538352.1:p.Leu1578Met
XM_011540051.1:c.4732C>A XP_011538353.1:p.Leu1578Met
XM_011540052.1:c.1060C>A XP_011538354.1:p.Leu354Met
XM_011540053.1:c.4732C>A XP_011538355.1:p.Leu1578Met
XR_945796.1:n.4975C>A
NM_022124.6:c.4537C>A MANE Select NP_071407.4:p.Leu1513Met