Canonical Allele Identifier: CA2554374852

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71708920_71708921insTCTGCT , CM000672.2:g.71708920_71708921insTCTGCT	GRCh38
NC_000010.10:g.73468677_73468678insTCTGCT , CM000672.1:g.73468677_73468678insTCTGCT	GRCh37
NC_000010.9:g.73138683_73138684insTCTGCT	NCBI36
NG_008835.1:g.316974_316975insTCTGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.3107-178_3107-177insTCTGCT MANE Select	ENSP00000224721.9:n.3107-178_3107-177insTCTGCT
ENST00000398809.9:c.3107-178_3107-177insTCTGCT	ENSP00000381789.5:n.3107-178_3107-177insTCTGCT
ENST00000442677.4:c.3107-178_3107-177insTCTGCT	ENSP00000388894.3:n.3107-178_3107-177insTCTGCT
ENST00000466757.8:c.2538-178_2538-177insTCTGCT
ENST00000224721.10:c.3122-178_3122-177insTCTGCT	ENSP00000224721.8:n.3122-178_3122-177insTCTGCT
ENST00000398809.8:c.3107-178_3107-177insTCTGCT	ENSP00000381789.5:n.3107-178_3107-177insTCTGCT
ENST00000442677.3:c.1882-178_1882-177insTCTGCT
ENST00000466757.7:c.2538-178_2538-177insTCTGCT
ENST00000616684.4:c.3107-178_3107-177insTCTGCT	ENSP00000482036.2:n.3107-178_3107-177insTCTGCT
ENST00000622827.4:c.3107-178_3107-177insTCTGCT	ENSP00000483211.1:n.3107-178_3107-177insTCTGCT
NM_001171930.1:c.3107-178_3107-177insTCTGCT	NP_001165401.1:n.3107-178_3107-177insTCTGCT
NM_022124.5:c.3107-178_3107-177insTCTGCT	NP_071407.4:n.3107-178_3107-177insTCTGCT
XM_006717940.2:c.3302-178_3302-177insTCTGCT	XP_006718003.1:n.3302-178_3302-177insTCTGCT
XM_006717942.2:c.3236-178_3236-177insTCTGCT	XP_006718005.1:n.3236-178_3236-177insTCTGCT
XM_011540039.1:c.3302-178_3302-177insTCTGCT	XP_011538341.1:n.3302-178_3302-177insTCTGCT
XM_011540040.1:c.3296-178_3296-177insTCTGCT	XP_011538342.1:n.3296-178_3296-177insTCTGCT
XM_011540041.1:c.3242-178_3242-177insTCTGCT	XP_011538343.1:n.3242-178_3242-177insTCTGCT
XM_011540042.1:c.3302-178_3302-177insTCTGCT	XP_011538344.1:n.3302-178_3302-177insTCTGCT
XM_011540043.1:c.3302-178_3302-177insTCTGCT	XP_011538345.1:n.3302-178_3302-177insTCTGCT
XM_011540044.1:c.3167-178_3167-177insTCTGCT	XP_011538346.1:n.3167-178_3167-177insTCTGCT
XM_011540045.1:c.3302-178_3302-177insTCTGCT	XP_011538347.1:n.3302-178_3302-177insTCTGCT
XM_011540046.1:c.2762-178_2762-177insTCTGCT	XP_011538348.1:n.2762-178_2762-177insTCTGCT
XM_011540047.1:c.2120-178_2120-177insTCTGCT	XP_011538349.1:n.2120-178_2120-177insTCTGCT
XM_011540048.1:c.3302-178_3302-177insTCTGCT	XP_011538350.1:n.3302-178_3302-177insTCTGCT
XM_011540049.1:c.3302-178_3302-177insTCTGCT	XP_011538351.1:n.3302-178_3302-177insTCTGCT
XM_011540050.1:c.3302-178_3302-177insTCTGCT	XP_011538352.1:n.3302-178_3302-177insTCTGCT
XM_011540051.1:c.3302-178_3302-177insTCTGCT	XP_011538353.1:n.3302-178_3302-177insTCTGCT
XM_011540053.1:c.3302-178_3302-177insTCTGCT	XP_011538355.1:n.3302-178_3302-177insTCTGCT
XR_945796.1:n.3545-178_3545-177insTCTGCT
XR_946052.1:n.82+85_82+86insAGCAGA
NM_001171930.2:c.3107-178_3107-177insTCTGCT	NP_001165401.1:n.3107-178_3107-177insTCTGCT
NM_022124.6:c.3107-178_3107-177insTCTGCT MANE Select	NP_071407.4:n.3107-178_3107-177insTCTGCT