Canonical Allele Identifier: CA2788480923
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71785158_71785159insAGA , CM000672.2:g.71785158_71785159insAGA GRCh38
NC_000010.10:g.73544915_73544916insAGA , CM000672.1:g.73544915_73544916insAGA GRCh37
NC_000010.9:g.73214921_73214922insAGA NCBI36
NG_008835.1:g.393212_393213insAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.5712+58_5712+59insAGA MANE Select ENSP00000224721.9:n.5712+58_5712+59insAGA
ENST00000224721.10:c.5727+58_5727+59insAGA ENSP00000224721.8:n.5727+58_5727+59insAGA
ENST00000622827.4:c.5712+58_5712+59insAGA ENSP00000483211.1:n.5712+58_5712+59insAGA
NM_022124.5:c.5712+58_5712+59insAGA NP_071407.4:n.5712+58_5712+59insAGA
XM_006717940.2:c.5907+58_5907+59insAGA XP_006718003.1:n.5907+58_5907+59insAGA
XM_006717942.2:c.5841+58_5841+59insAGA XP_006718005.1:n.5841+58_5841+59insAGA
XM_011540039.1:c.5904+58_5904+59insAGA XP_011538341.1:n.5904+58_5904+59insAGA
XM_011540040.1:c.5901+58_5901+59insAGA XP_011538342.1:n.5901+58_5901+59insAGA
XM_011540041.1:c.5847+58_5847+59insAGA XP_011538343.1:n.5847+58_5847+59insAGA
XM_011540042.1:c.5907+58_5907+59insAGA XP_011538344.1:n.5907+58_5907+59insAGA
XM_011540043.1:c.5907+58_5907+59insAGA XP_011538345.1:n.5907+58_5907+59insAGA
XM_011540044.1:c.5772+58_5772+59insAGA XP_011538346.1:n.5772+58_5772+59insAGA
XM_011540045.1:c.5907+58_5907+59insAGA XP_011538347.1:n.5907+58_5907+59insAGA
XM_011540046.1:c.5367+58_5367+59insAGA XP_011538348.1:n.5367+58_5367+59insAGA
XM_011540047.1:c.4725+58_4725+59insAGA XP_011538349.1:n.4725+58_4725+59insAGA
XM_011540048.1:c.5907+58_5907+59insAGA XP_011538350.1:n.5907+58_5907+59insAGA
XM_011540049.1:c.5907+58_5907+59insAGA XP_011538351.1:n.5907+58_5907+59insAGA
XM_011540050.1:c.5907+58_5907+59insAGA XP_011538352.1:n.5907+58_5907+59insAGA
XM_011540051.1:c.5907+58_5907+59insAGA XP_011538353.1:n.5907+58_5907+59insAGA
XM_011540052.1:c.2235+58_2235+59insAGA XP_011538354.1:n.2235+58_2235+59insAGA
XM_011540053.1:c.5907+58_5907+59insAGA XP_011538355.1:n.5907+58_5907+59insAGA
XR_945796.1:n.6150+58_6150+59insAGA
NM_022124.6:c.5712+58_5712+59insAGA MANE Select NP_071407.4:n.5712+58_5712+59insAGA