Canonical Allele Identifier: CA1918853839
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71740857G= , CM000672.2:g.71740857G= GRCh38
NC_000010.10:g.73500614G= , CM000672.1:g.73500614G= GRCh37
NC_000010.9:g.73170620G= NCBI36
NG_008835.1:g.348911G=

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.4524G= MANE Select ENSP00000224721.9:p.Lys1508=
ENST00000224721.10:c.4539G= ENSP00000224721.8:p.Lys1513=
ENST00000398792.3:n.1213G=
ENST00000622827.4:c.4524G= ENSP00000483211.1:p.Lys1508=
NM_022124.5:c.4524G= NP_071407.4:p.Lys1508=
XM_006717940.2:c.4719G= XP_006718003.1:p.Lys1573=
XM_006717942.2:c.4653G= XP_006718005.1:p.Lys1551=
XM_011540039.1:c.4716G= XP_011538341.1:p.Lys1572=
XM_011540040.1:c.4713G= XP_011538342.1:p.Lys1571=
XM_011540041.1:c.4659G= XP_011538343.1:p.Lys1553=
XM_011540042.1:c.4719G= XP_011538344.1:p.Lys1573=
XM_011540043.1:c.4719G= XP_011538345.1:p.Lys1573=
XM_011540044.1:c.4584G= XP_011538346.1:p.Lys1528=
XM_011540045.1:c.4719G= XP_011538347.1:p.Lys1573=
XM_011540046.1:c.4179G= XP_011538348.1:p.Lys1393=
XM_011540047.1:c.3537G= XP_011538349.1:p.Lys1179=
XM_011540048.1:c.4719G= XP_011538350.1:p.Lys1573=
XM_011540049.1:c.4719G= XP_011538351.1:p.Lys1573=
XM_011540050.1:c.4719G= XP_011538352.1:p.Lys1573=
XM_011540051.1:c.4719G= XP_011538353.1:p.Lys1573=
XM_011540052.1:c.1047G= XP_011538354.1:p.Lys349=
XM_011540053.1:c.4719G= XP_011538355.1:p.Lys1573=
XR_945796.1:n.4962G=
NM_022124.6:c.4524G= MANE Select NP_071407.4:p.Lys1508=