Canonical Allele Identifier: CA2788480946
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71785173_71785174insAG , CM000672.2:g.71785173_71785174insAG GRCh38
NC_000010.10:g.73544930_73544931insAG , CM000672.1:g.73544930_73544931insAG GRCh37
NC_000010.9:g.73214936_73214937insAG NCBI36
NG_008835.1:g.393227_393228insAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.5712+73_5712+74insAG MANE Select ENSP00000224721.9:n.5712+73_5712+74insAG
ENST00000224721.10:c.5727+73_5727+74insAG ENSP00000224721.8:n.5727+73_5727+74insAG
ENST00000622827.4:c.5712+73_5712+74insAG ENSP00000483211.1:n.5712+73_5712+74insAG
NM_022124.5:c.5712+73_5712+74insAG NP_071407.4:n.5712+73_5712+74insAG
XM_006717940.2:c.5907+73_5907+74insAG XP_006718003.1:n.5907+73_5907+74insAG
XM_006717942.2:c.5841+73_5841+74insAG XP_006718005.1:n.5841+73_5841+74insAG
XM_011540039.1:c.5904+73_5904+74insAG XP_011538341.1:n.5904+73_5904+74insAG
XM_011540040.1:c.5901+73_5901+74insAG XP_011538342.1:n.5901+73_5901+74insAG
XM_011540041.1:c.5847+73_5847+74insAG XP_011538343.1:n.5847+73_5847+74insAG
XM_011540042.1:c.5907+73_5907+74insAG XP_011538344.1:n.5907+73_5907+74insAG
XM_011540043.1:c.5907+73_5907+74insAG XP_011538345.1:n.5907+73_5907+74insAG
XM_011540044.1:c.5772+73_5772+74insAG XP_011538346.1:n.5772+73_5772+74insAG
XM_011540045.1:c.5907+73_5907+74insAG XP_011538347.1:n.5907+73_5907+74insAG
XM_011540046.1:c.5367+73_5367+74insAG XP_011538348.1:n.5367+73_5367+74insAG
XM_011540047.1:c.4725+73_4725+74insAG XP_011538349.1:n.4725+73_4725+74insAG
XM_011540048.1:c.5907+73_5907+74insAG XP_011538350.1:n.5907+73_5907+74insAG
XM_011540049.1:c.5907+73_5907+74insAG XP_011538351.1:n.5907+73_5907+74insAG
XM_011540050.1:c.5907+73_5907+74insAG XP_011538352.1:n.5907+73_5907+74insAG
XM_011540051.1:c.5907+73_5907+74insAG XP_011538353.1:n.5907+73_5907+74insAG
XM_011540052.1:c.2235+73_2235+74insAG XP_011538354.1:n.2235+73_2235+74insAG
XM_011540053.1:c.5907+73_5907+74insAG XP_011538355.1:n.5907+73_5907+74insAG
XR_945796.1:n.6150+73_6150+74insAG
NM_022124.6:c.5712+73_5712+74insAG MANE Select NP_071407.4:n.5712+73_5712+74insAG