Canonical Allele Identifier: CA2788479408

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71709332_71709333insA , CM000672.2:g.71709332_71709333insA	GRCh38
NC_000010.10:g.73469089_73469090insA , CM000672.1:g.73469089_73469090insA	GRCh37
NC_000010.9:g.73139095_73139096insA	NCBI36
NG_008835.1:g.317386_317387insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.3220+121_3220+122insA MANE Select	ENSP00000224721.9:n.3220+121_3220+122insA
ENST00000398809.9:c.3220+121_3220+122insA	ENSP00000381789.5:n.3220+121_3220+122insA
ENST00000442677.4:c.3220+121_3220+122insA	ENSP00000388894.3:n.3220+121_3220+122insA
ENST00000466757.8:c.2651+121_2651+122insA
ENST00000224721.10:c.3235+121_3235+122insA	ENSP00000224721.8:n.3235+121_3235+122insA
ENST00000398809.8:c.3220+121_3220+122insA	ENSP00000381789.5:n.3220+121_3220+122insA
ENST00000442677.3:c.1995+121_1995+122insA
ENST00000466757.7:c.2651+121_2651+122insA
ENST00000616684.4:c.3220+121_3220+122insA	ENSP00000482036.2:n.3220+121_3220+122insA
ENST00000622827.4:c.3220+121_3220+122insA	ENSP00000483211.1:n.3220+121_3220+122insA
NM_001171930.1:c.3220+121_3220+122insA	NP_001165401.1:n.3220+121_3220+122insA
NM_022124.5:c.3220+121_3220+122insA	NP_071407.4:n.3220+121_3220+122insA
XM_006717940.2:c.3415+121_3415+122insA	XP_006718003.1:n.3415+121_3415+122insA
XM_006717942.2:c.3349+121_3349+122insA	XP_006718005.1:n.3349+121_3349+122insA
XM_011540039.1:c.3415+121_3415+122insA	XP_011538341.1:n.3415+121_3415+122insA
XM_011540040.1:c.3409+121_3409+122insA	XP_011538342.1:n.3409+121_3409+122insA
XM_011540041.1:c.3355+121_3355+122insA	XP_011538343.1:n.3355+121_3355+122insA
XM_011540042.1:c.3415+121_3415+122insA	XP_011538344.1:n.3415+121_3415+122insA
XM_011540043.1:c.3415+121_3415+122insA	XP_011538345.1:n.3415+121_3415+122insA
XM_011540044.1:c.3280+121_3280+122insA	XP_011538346.1:n.3280+121_3280+122insA
XM_011540045.1:c.3415+121_3415+122insA	XP_011538347.1:n.3415+121_3415+122insA
XM_011540046.1:c.2875+121_2875+122insA	XP_011538348.1:n.2875+121_2875+122insA
XM_011540047.1:c.2233+121_2233+122insA	XP_011538349.1:n.2233+121_2233+122insA
XM_011540048.1:c.3415+121_3415+122insA	XP_011538350.1:n.3415+121_3415+122insA
XM_011540049.1:c.3415+121_3415+122insA	XP_011538351.1:n.3415+121_3415+122insA
XM_011540050.1:c.3415+121_3415+122insA	XP_011538352.1:n.3415+121_3415+122insA
XM_011540051.1:c.3415+121_3415+122insA	XP_011538353.1:n.3415+121_3415+122insA
XM_011540053.1:c.3415+121_3415+122insA	XP_011538355.1:n.3415+121_3415+122insA
XR_945796.1:n.3658+121_3658+122insA
NM_001171930.2:c.3220+121_3220+122insA	NP_001165401.1:n.3220+121_3220+122insA
NM_022124.6:c.3220+121_3220+122insA MANE Select	NP_071407.4:n.3220+121_3220+122insA