Canonical Allele Identifier: CA1918837865
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71706856C= , CM000672.2:g.71706856C= GRCh38
NC_000010.10:g.73466613C= , CM000672.1:g.73466613C= GRCh37
NC_000010.9:g.73136619C= NCBI36
NG_008835.1:g.314910C=

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.2954-41C= MANE Select ENSP00000224721.9:n.2954-41C=
ENST00000398809.9:c.2954-41C= ENSP00000381789.5:n.2954-41C=
ENST00000442677.4:c.2954-41C= ENSP00000388894.3:n.2954-41C=
ENST00000466757.8:c.2385-41C=
ENST00000224721.10:c.2969-41C= ENSP00000224721.8:n.2969-41C=
ENST00000299366.11:c.2954-41C= ENSP00000299366.8:n.2954-41C=
ENST00000398809.8:c.2954-41C= ENSP00000381789.5:n.2954-41C=
ENST00000442677.3:c.1729-41C=
ENST00000466757.7:c.2385-41C=
ENST00000616684.4:c.2954-41C= ENSP00000482036.2:n.2954-41C=
ENST00000622827.4:c.2954-41C= ENSP00000483211.1:n.2954-41C=
NM_001171930.1:c.2954-41C= NP_001165401.1:n.2954-41C=
NM_001171931.1:c.2954-41C= NP_001165402.1:n.2954-41C=
NM_022124.5:c.2954-41C= NP_071407.4:n.2954-41C=
XM_006717940.2:c.3149-41C= XP_006718003.1:n.3149-41C=
XM_006717942.2:c.3083-41C= XP_006718005.1:n.3083-41C=
XM_011540039.1:c.3149-41C= XP_011538341.1:n.3149-41C=
XM_011540040.1:c.3143-41C= XP_011538342.1:n.3143-41C=
XM_011540041.1:c.3089-41C= XP_011538343.1:n.3089-41C=
XM_011540042.1:c.3149-41C= XP_011538344.1:n.3149-41C=
XM_011540043.1:c.3149-41C= XP_011538345.1:n.3149-41C=
XM_011540044.1:c.3014-41C= XP_011538346.1:n.3014-41C=
XM_011540045.1:c.3149-41C= XP_011538347.1:n.3149-41C=
XM_011540046.1:c.2609-41C= XP_011538348.1:n.2609-41C=
XM_011540047.1:c.1967-41C= XP_011538349.1:n.1967-41C=
XM_011540048.1:c.3149-41C= XP_011538350.1:n.3149-41C=
XM_011540049.1:c.3149-41C= XP_011538351.1:n.3149-41C=
XM_011540050.1:c.3149-41C= XP_011538352.1:n.3149-41C=
XM_011540051.1:c.3149-41C= XP_011538353.1:n.3149-41C=
XM_011540053.1:c.3149-41C= XP_011538355.1:n.3149-41C=
XM_011540054.1:c.3089-41C= XP_011538356.1:n.3089-41C=
XR_945796.1:n.3392-41C=
XR_946052.1:n.82+2150G=
NM_001171930.2:c.2954-41C= NP_001165401.1:n.2954-41C=
NM_001171931.2:c.2954-41C= NP_001165402.1:n.2954-41C=
NM_022124.6:c.2954-41C= MANE Select NP_071407.4:n.2954-41C=