Canonical Allele Identifier: CA5544189

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71695496A>G , CM000672.2:g.71695496A>G	GRCh38
NC_000010.10:g.73455253A>G , CM000672.1:g.73455253A>G	GRCh37
NC_000010.9:g.73125259A>G	NCBI36
NG_008835.1:g.303550A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.2368A>G MANE Select	ENSP00000224721.9:p.Met790Val
ENST00000398809.9:c.2368A>G	ENSP00000381789.5:p.Met790Val
ENST00000442677.4:c.2368A>G	ENSP00000388894.3:p.Met790Val
ENST00000466757.8:c.1799A>G
ENST00000224721.10:c.2383A>G	ENSP00000224721.8:p.Met795Val
ENST00000299366.11:c.2368A>G	ENSP00000299366.8:p.Met790Val
ENST00000398809.8:c.2368A>G	ENSP00000381789.5:p.Met790Val
ENST00000442677.3:c.1143A>G
ENST00000466757.7:c.1799A>G
ENST00000616684.4:c.2368A>G	ENSP00000482036.2:p.Met790Val
ENST00000622827.4:c.2368A>G	ENSP00000483211.1:p.Met790Val
NM_001171930.1:c.2368A>G	NP_001165401.1:p.Met790Val
NM_001171931.1:c.2368A>G	NP_001165402.1:p.Met790Val
NM_022124.5:c.2368A>G	NP_071407.4:p.Met790Val
XM_006717940.2:c.2563A>G	XP_006718003.1:p.Met855Val
XM_006717942.2:c.2497A>G	XP_006718005.1:p.Met833Val
XM_011540039.1:c.2563A>G	XP_011538341.1:p.Met855Val
XM_011540040.1:c.2557A>G	XP_011538342.1:p.Met853Val
XM_011540041.1:c.2503A>G	XP_011538343.1:p.Met835Val
XM_011540042.1:c.2563A>G	XP_011538344.1:p.Met855Val
XM_011540043.1:c.2563A>G	XP_011538345.1:p.Met855Val
XM_011540044.1:c.2428A>G	XP_011538346.1:p.Met810Val
XM_011540045.1:c.2563A>G	XP_011538347.1:p.Met855Val
XM_011540046.1:c.2023A>G	XP_011538348.1:p.Met675Val
XM_011540047.1:c.1381A>G	XP_011538349.1:p.Met461Val
XM_011540048.1:c.2563A>G	XP_011538350.1:p.Met855Val
XM_011540049.1:c.2563A>G	XP_011538351.1:p.Met855Val
XM_011540050.1:c.2563A>G	XP_011538352.1:p.Met855Val
XM_011540051.1:c.2563A>G	XP_011538353.1:p.Met855Val
XM_011540053.1:c.2563A>G	XP_011538355.1:p.Met855Val
XM_011540054.1:c.2503A>G	XP_011538356.1:p.Met835Val
XR_945796.1:n.2806A>G
NM_001171930.2:c.2368A>G	NP_001165401.1:p.Met790Val
NM_001171931.2:c.2368A>G	NP_001165402.1:p.Met790Val
NM_022124.6:c.2368A>G MANE Select	NP_071407.4:p.Met790Val