Canonical Allele Identifier: CA1918853823

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740831T= , CM000672.2:g.71740831T=	GRCh38
NC_000010.10:g.73500588T= , CM000672.1:g.73500588T=	GRCh37
NC_000010.9:g.73170594T=	NCBI36
NG_008835.1:g.348885T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4498T= MANE Select	ENSP00000224721.9:p.Ser1500=
ENST00000224721.10:c.4513T=	ENSP00000224721.8:p.Ser1505=
ENST00000398792.3:n.1187T=
ENST00000622827.4:c.4498T=	ENSP00000483211.1:p.Ser1500=
NM_022124.5:c.4498T=	NP_071407.4:p.Ser1500=
XM_006717940.2:c.4693T=	XP_006718003.1:p.Ser1565=
XM_006717942.2:c.4627T=	XP_006718005.1:p.Ser1543=
XM_011540039.1:c.4690T=	XP_011538341.1:p.Ser1564=
XM_011540040.1:c.4687T=	XP_011538342.1:p.Ser1563=
XM_011540041.1:c.4633T=	XP_011538343.1:p.Ser1545=
XM_011540042.1:c.4693T=	XP_011538344.1:p.Ser1565=
XM_011540043.1:c.4693T=	XP_011538345.1:p.Ser1565=
XM_011540044.1:c.4558T=	XP_011538346.1:p.Ser1520=
XM_011540045.1:c.4693T=	XP_011538347.1:p.Ser1565=
XM_011540046.1:c.4153T=	XP_011538348.1:p.Ser1385=
XM_011540047.1:c.3511T=	XP_011538349.1:p.Ser1171=
XM_011540048.1:c.4693T=	XP_011538350.1:p.Ser1565=
XM_011540049.1:c.4693T=	XP_011538351.1:p.Ser1565=
XM_011540050.1:c.4693T=	XP_011538352.1:p.Ser1565=
XM_011540051.1:c.4693T=	XP_011538353.1:p.Ser1565=
XM_011540052.1:c.1021T=	XP_011538354.1:p.Ser341=
XM_011540053.1:c.4693T=	XP_011538355.1:p.Ser1565=
XR_945796.1:n.4936T=
NM_022124.6:c.4498T= MANE Select	NP_071407.4:p.Ser1500=