Canonical Allele Identifier: CA1918870157
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71790316C= , CM000672.2:g.71790316C= GRCh38
NC_000010.10:g.73550073C= , CM000672.1:g.73550073C= GRCh37
NC_000010.9:g.73220079C= NCBI36
NG_008835.1:g.398370C=

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.5952C= MANE Select ENSP00000224721.9:p.Pro1984=
ENST00000224721.10:c.5967C= ENSP00000224721.8:p.Pro1989=
ENST00000622827.4:c.5952C= ENSP00000483211.1:p.Pro1984=
NM_022124.5:c.5952C= NP_071407.4:p.Pro1984=
XM_006717940.2:c.6147C= XP_006718003.1:p.Pro2049=
XM_006717942.2:c.6081C= XP_006718005.1:p.Pro2027=
XM_011540039.1:c.6144C= XP_011538341.1:p.Pro2048=
XM_011540040.1:c.6141C= XP_011538342.1:p.Pro2047=
XM_011540041.1:c.6087C= XP_011538343.1:p.Pro2029=
XM_011540042.1:c.6147C= XP_011538344.1:p.Pro2049=
XM_011540043.1:c.6147C= XP_011538345.1:p.Pro2049=
XM_011540044.1:c.6012C= XP_011538346.1:p.Pro2004=
XM_011540045.1:c.6147C= XP_011538347.1:p.Pro2049=
XM_011540046.1:c.5607C= XP_011538348.1:p.Pro1869=
XM_011540047.1:c.4965C= XP_011538349.1:p.Pro1655=
XM_011540048.1:c.6147C= XP_011538350.1:p.Pro2049=
XM_011540049.1:c.6147C= XP_011538351.1:p.Pro2049=
XM_011540050.1:c.6147C= XP_011538352.1:p.Pro2049=
XM_011540051.1:c.6147C= XP_011538353.1:p.Pro2049=
XM_011540052.1:c.2475C= XP_011538354.1:p.Pro825=
XR_945796.1:n.6390C=
NM_022124.6:c.5952C= MANE Select NP_071407.4:p.Pro1984=