Canonical Allele Identifier: CA2788479417

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71709362_71709363insACC , CM000672.2:g.71709362_71709363insACC	GRCh38
NC_000010.10:g.73469119_73469120insACC , CM000672.1:g.73469119_73469120insACC	GRCh37
NC_000010.9:g.73139125_73139126insACC	NCBI36
NG_008835.1:g.317416_317417insACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.3220+151_3220+152insACC MANE Select	ENSP00000224721.9:n.3220+151_3220+152insACC
ENST00000398809.9:c.3220+151_3220+152insACC	ENSP00000381789.5:n.3220+151_3220+152insACC
ENST00000442677.4:c.3220+151_3220+152insACC	ENSP00000388894.3:n.3220+151_3220+152insACC
ENST00000466757.8:c.2651+151_2651+152insACC
ENST00000224721.10:c.3235+151_3235+152insACC	ENSP00000224721.8:n.3235+151_3235+152insACC
ENST00000398809.8:c.3220+151_3220+152insACC	ENSP00000381789.5:n.3220+151_3220+152insACC
ENST00000442677.3:c.1995+151_1995+152insACC
ENST00000466757.7:c.2651+151_2651+152insACC
ENST00000616684.4:c.3220+151_3220+152insACC	ENSP00000482036.2:n.3220+151_3220+152insACC
ENST00000622827.4:c.3220+151_3220+152insACC	ENSP00000483211.1:n.3220+151_3220+152insACC
NM_001171930.1:c.3220+151_3220+152insACC	NP_001165401.1:n.3220+151_3220+152insACC
NM_022124.5:c.3220+151_3220+152insACC	NP_071407.4:n.3220+151_3220+152insACC
XM_006717940.2:c.3415+151_3415+152insACC	XP_006718003.1:n.3415+151_3415+152insACC
XM_006717942.2:c.3349+151_3349+152insACC	XP_006718005.1:n.3349+151_3349+152insACC
XM_011540039.1:c.3415+151_3415+152insACC	XP_011538341.1:n.3415+151_3415+152insACC
XM_011540040.1:c.3409+151_3409+152insACC	XP_011538342.1:n.3409+151_3409+152insACC
XM_011540041.1:c.3355+151_3355+152insACC	XP_011538343.1:n.3355+151_3355+152insACC
XM_011540042.1:c.3415+151_3415+152insACC	XP_011538344.1:n.3415+151_3415+152insACC
XM_011540043.1:c.3415+151_3415+152insACC	XP_011538345.1:n.3415+151_3415+152insACC
XM_011540044.1:c.3280+151_3280+152insACC	XP_011538346.1:n.3280+151_3280+152insACC
XM_011540045.1:c.3415+151_3415+152insACC	XP_011538347.1:n.3415+151_3415+152insACC
XM_011540046.1:c.2875+151_2875+152insACC	XP_011538348.1:n.2875+151_2875+152insACC
XM_011540047.1:c.2233+151_2233+152insACC	XP_011538349.1:n.2233+151_2233+152insACC
XM_011540048.1:c.3415+151_3415+152insACC	XP_011538350.1:n.3415+151_3415+152insACC
XM_011540049.1:c.3415+151_3415+152insACC	XP_011538351.1:n.3415+151_3415+152insACC
XM_011540050.1:c.3415+151_3415+152insACC	XP_011538352.1:n.3415+151_3415+152insACC
XM_011540051.1:c.3415+151_3415+152insACC	XP_011538353.1:n.3415+151_3415+152insACC
XM_011540053.1:c.3415+151_3415+152insACC	XP_011538355.1:n.3415+151_3415+152insACC
XR_945796.1:n.3658+151_3658+152insACC
NM_001171930.2:c.3220+151_3220+152insACC	NP_001165401.1:n.3220+151_3220+152insACC
NM_022124.6:c.3220+151_3220+152insACC MANE Select	NP_071407.4:n.3220+151_3220+152insACC