Canonical Allele Identifier: CA1918874208
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71793272_71793273delinsGC , CM000672.2:g.71793272_71793273delinsGC GRCh38
NC_000010.10:g.73553029_73553030delinsGC , CM000672.1:g.73553029_73553030delinsGC GRCh37
NC_000010.9:g.73223035_73223036delinsGC NCBI36
NG_008835.1:g.401326_401327delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.6344_6345delinsGC MANE Select ENSP00000224721.9:p.Arg2115=
ENST00000224721.10:c.6359_6360delinsGC ENSP00000224721.8:p.Arg2120=
ENST00000622827.4:c.6344_6345delinsGC ENSP00000483211.1:p.Arg2115=
NM_022124.5:c.6344_6345delinsGC NP_071407.4:p.Arg2115=
XM_006717940.2:c.6539_6540delinsGC XP_006718003.1:p.Arg2180=
XM_006717942.2:c.6473_6474delinsGC XP_006718005.1:p.Arg2158=
XM_011540039.1:c.6536_6537delinsGC XP_011538341.1:p.Arg2179=
XM_011540040.1:c.6533_6534delinsGC XP_011538342.1:p.Arg2178=
XM_011540041.1:c.6479_6480delinsGC XP_011538343.1:p.Arg2160=
XM_011540042.1:c.6539_6540delinsGC XP_011538344.1:p.Arg2180=
XM_011540043.1:c.6539_6540delinsGC XP_011538345.1:p.Arg2180=
XM_011540044.1:c.6404_6405delinsGC XP_011538346.1:p.Arg2135=
XM_011540045.1:c.6539_6540delinsGC XP_011538347.1:p.Arg2180=
XM_011540046.1:c.5999_6000delinsGC XP_011538348.1:p.Arg2000=
XM_011540047.1:c.5357_5358delinsGC XP_011538349.1:p.Arg1786=
XM_011540048.1:c.6539_6540delinsGC XP_011538350.1:p.Arg2180=
XM_011540049.1:c.6539_6540delinsGC XP_011538351.1:p.Arg2180=
XM_011540050.1:c.6539_6540delinsGC XP_011538352.1:p.Arg2180=
XM_011540051.1:c.6539_6540delinsGC XP_011538353.1:p.Arg2180=
XM_011540052.1:c.2867_2868delinsGC XP_011538354.1:p.Arg956=
XR_945796.1:n.6782_6783delinsGC
NM_022124.6:c.6344_6345delinsGC MANE Select NP_071407.4:p.Arg2115=