Canonical Allele Identifier: CA1918874292

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793351G= , CM000672.2:g.71793351G=	GRCh38
NC_000010.10:g.73553108G= , CM000672.1:g.73553108G=	GRCh37
NC_000010.9:g.73223114G=	NCBI36
NG_008835.1:g.401405G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6423G= MANE Select	ENSP00000224721.9:p.Arg2141=
ENST00000224721.10:c.6438G=	ENSP00000224721.8:p.Arg2146=
ENST00000622827.4:c.6423G=	ENSP00000483211.1:p.Arg2141=
NM_022124.5:c.6423G=	NP_071407.4:p.Arg2141=
XM_006717940.2:c.6618G=	XP_006718003.1:p.Arg2206=
XM_006717942.2:c.6552G=	XP_006718005.1:p.Arg2184=
XM_011540039.1:c.6615G=	XP_011538341.1:p.Arg2205=
XM_011540040.1:c.6612G=	XP_011538342.1:p.Arg2204=
XM_011540041.1:c.6558G=	XP_011538343.1:p.Arg2186=
XM_011540042.1:c.6577+41G=	XP_011538344.1:n.6577+41G=
XM_011540043.1:c.6618G=	XP_011538345.1:p.Arg2206=
XM_011540044.1:c.6483G=	XP_011538346.1:p.Arg2161=
XM_011540045.1:c.6618G=	XP_011538347.1:p.Arg2206=
XM_011540046.1:c.6078G=	XP_011538348.1:p.Arg2026=
XM_011540047.1:c.5436G=	XP_011538349.1:p.Arg1812=
XM_011540048.1:c.6618G=	XP_011538350.1:p.Arg2206=
XM_011540049.1:c.6618G=	XP_011538351.1:p.Arg2206=
XM_011540050.1:c.6618G=	XP_011538352.1:p.Arg2206=
XM_011540051.1:c.6618G=	XP_011538353.1:p.Arg2206=
XM_011540052.1:c.2946G=	XP_011538354.1:p.Arg982=
XR_945796.1:n.6861G=
NM_022124.6:c.6423G= MANE Select	NP_071407.4:p.Arg2141=