Canonical Allele Identifier: CA1918874252

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793319_71793320delinsAC , CM000672.2:g.71793319_71793320delinsAC	GRCh38
NC_000010.10:g.73553076_73553077delinsAC , CM000672.1:g.73553076_73553077delinsAC	GRCh37
NC_000010.9:g.73223082_73223083delinsAC	NCBI36
NG_008835.1:g.401373_401374delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6391_6392delinsAC MANE Select	ENSP00000224721.9:p.Thr2131=
ENST00000224721.10:c.6406_6407delinsAC	ENSP00000224721.8:p.Thr2136=
ENST00000622827.4:c.6391_6392delinsAC	ENSP00000483211.1:p.Thr2131=
NM_022124.5:c.6391_6392delinsAC	NP_071407.4:p.Thr2131=
XM_006717940.2:c.6586_6587delinsAC	XP_006718003.1:p.Thr2196=
XM_006717942.2:c.6520_6521delinsAC	XP_006718005.1:p.Thr2174=
XM_011540039.1:c.6583_6584delinsAC	XP_011538341.1:p.Thr2195=
XM_011540040.1:c.6580_6581delinsAC	XP_011538342.1:p.Thr2194=
XM_011540041.1:c.6526_6527delinsAC	XP_011538343.1:p.Thr2176=
XM_011540042.1:c.6577+9_6577+10delinsAC	XP_011538344.1:n.6577+9_6577+10delinsAC
XM_011540043.1:c.6586_6587delinsAC	XP_011538345.1:p.Thr2196=
XM_011540044.1:c.6451_6452delinsAC	XP_011538346.1:p.Thr2151=
XM_011540045.1:c.6586_6587delinsAC	XP_011538347.1:p.Thr2196=
XM_011540046.1:c.6046_6047delinsAC	XP_011538348.1:p.Thr2016=
XM_011540047.1:c.5404_5405delinsAC	XP_011538349.1:p.Thr1802=
XM_011540048.1:c.6586_6587delinsAC	XP_011538350.1:p.Thr2196=
XM_011540049.1:c.6586_6587delinsAC	XP_011538351.1:p.Thr2196=
XM_011540050.1:c.6586_6587delinsAC	XP_011538352.1:p.Thr2196=
XM_011540051.1:c.6586_6587delinsAC	XP_011538353.1:p.Thr2196=
XM_011540052.1:c.2914_2915delinsAC	XP_011538354.1:p.Thr972=
XR_945796.1:n.6829_6830delinsAC
NM_022124.6:c.6391_6392delinsAC MANE Select	NP_071407.4:p.Thr2131=