Canonical Allele Identifier: CA2695212171
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71793320_71793321insA , CM000672.2:g.71793320_71793321insA GRCh38
NC_000010.10:g.73553077_73553078insA , CM000672.1:g.73553077_73553078insA GRCh37
NC_000010.9:g.73223083_73223084insA NCBI36
NG_008835.1:g.401374_401375insA

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.6392_6393insA MANE Select ENSP00000224721.9:p.Ile2132HisfsTer?
ENST00000224721.10:c.6407_6408insA ENSP00000224721.8:p.Ile2137HisfsTer?
ENST00000622827.4:c.6392_6393insA ENSP00000483211.1:p.Ile2132HisfsTer?
NM_022124.5:c.6392_6393insA NP_071407.4:p.Ile2132HisfsTer?
XM_006717940.2:c.6587_6588insA XP_006718003.1:p.Ile2197HisfsTer?
XM_006717942.2:c.6521_6522insA XP_006718005.1:p.Ile2175HisfsTer?
XM_011540039.1:c.6584_6585insA XP_011538341.1:p.Ile2196HisfsTer?
XM_011540040.1:c.6581_6582insA XP_011538342.1:p.Ile2195HisfsTer?
XM_011540041.1:c.6527_6528insA XP_011538343.1:p.Ile2177HisfsTer?
XM_011540042.1:c.6577+10_6577+11insA XP_011538344.1:n.6577+10_6577+11insA
XM_011540043.1:c.6587_6588insA XP_011538345.1:p.Ile2197HisfsTer?
XM_011540044.1:c.6452_6453insA XP_011538346.1:p.Ile2152HisfsTer?
XM_011540045.1:c.6587_6588insA XP_011538347.1:p.Ile2197HisfsTer?
XM_011540046.1:c.6047_6048insA XP_011538348.1:p.Ile2017HisfsTer?
XM_011540047.1:c.5405_5406insA XP_011538349.1:p.Ile1803HisfsTer?
XM_011540048.1:c.6587_6588insA XP_011538350.1:p.Ile2197HisfsTer?
XM_011540049.1:c.6587_6588insA XP_011538351.1:p.Ile2197HisfsTer?
XM_011540050.1:c.6587_6588insA XP_011538352.1:p.Ile2197HisfsTer?
XM_011540051.1:c.6587_6588insA XP_011538353.1:p.Ile2197HisfsTer?
XM_011540052.1:c.2915_2916insA XP_011538354.1:p.Ile973HisfsTer?
XR_945796.1:n.6830_6831insA
NM_022124.6:c.6392_6393insA MANE Select NP_071407.4:p.Ile2132HisfsTer?