Canonical Allele Identifier: CA1918853841

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740865A= , CM000672.2:g.71740865A=	GRCh38
NC_000010.10:g.73500622A= , CM000672.1:g.73500622A=	GRCh37
NC_000010.9:g.73170628A=	NCBI36
NG_008835.1:g.348919A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.4532A= MANE Select	ENSP00000224721.9:p.His1511=
ENST00000224721.10:c.4547A=	ENSP00000224721.8:p.His1516=
ENST00000398792.3:n.1221A=
ENST00000622827.4:c.4532A=	ENSP00000483211.1:p.His1511=
NM_022124.5:c.4532A=	NP_071407.4:p.His1511=
XM_006717940.2:c.4727A=	XP_006718003.1:p.His1576=
XM_006717942.2:c.4661A=	XP_006718005.1:p.His1554=
XM_011540039.1:c.4724A=	XP_011538341.1:p.His1575=
XM_011540040.1:c.4721A=	XP_011538342.1:p.His1574=
XM_011540041.1:c.4667A=	XP_011538343.1:p.His1556=
XM_011540042.1:c.4727A=	XP_011538344.1:p.His1576=
XM_011540043.1:c.4727A=	XP_011538345.1:p.His1576=
XM_011540044.1:c.4592A=	XP_011538346.1:p.His1531=
XM_011540045.1:c.4727A=	XP_011538347.1:p.His1576=
XM_011540046.1:c.4187A=	XP_011538348.1:p.His1396=
XM_011540047.1:c.3545A=	XP_011538349.1:p.His1182=
XM_011540048.1:c.4727A=	XP_011538350.1:p.His1576=
XM_011540049.1:c.4727A=	XP_011538351.1:p.His1576=
XM_011540050.1:c.4727A=	XP_011538352.1:p.His1576=
XM_011540051.1:c.4727A=	XP_011538353.1:p.His1576=
XM_011540052.1:c.1055A=	XP_011538354.1:p.His352=
XM_011540053.1:c.4727A=	XP_011538355.1:p.His1576=
XR_945796.1:n.4970A=
NM_022124.6:c.4532A= MANE Select	NP_071407.4:p.His1511=