Canonical Allele Identifier: CA1918874162

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793240G= , CM000672.2:g.71793240G=	GRCh38
NC_000010.10:g.73552997G= , CM000672.1:g.73552997G=	GRCh37
NC_000010.9:g.73223003G=	NCBI36
NG_008835.1:g.401294G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6312G= MANE Select	ENSP00000224721.9:p.Leu2104=
ENST00000224721.10:c.6327G=	ENSP00000224721.8:p.Leu2109=
ENST00000622827.4:c.6312G=	ENSP00000483211.1:p.Leu2104=
NM_022124.5:c.6312G=	NP_071407.4:p.Leu2104=
XM_006717940.2:c.6507G=	XP_006718003.1:p.Leu2169=
XM_006717942.2:c.6441G=	XP_006718005.1:p.Leu2147=
XM_011540039.1:c.6504G=	XP_011538341.1:p.Leu2168=
XM_011540040.1:c.6501G=	XP_011538342.1:p.Leu2167=
XM_011540041.1:c.6447G=	XP_011538343.1:p.Leu2149=
XM_011540042.1:c.6507G=	XP_011538344.1:p.Leu2169=
XM_011540043.1:c.6507G=	XP_011538345.1:p.Leu2169=
XM_011540044.1:c.6372G=	XP_011538346.1:p.Leu2124=
XM_011540045.1:c.6507G=	XP_011538347.1:p.Leu2169=
XM_011540046.1:c.5967G=	XP_011538348.1:p.Leu1989=
XM_011540047.1:c.5325G=	XP_011538349.1:p.Leu1775=
XM_011540048.1:c.6507G=	XP_011538350.1:p.Leu2169=
XM_011540049.1:c.6507G=	XP_011538351.1:p.Leu2169=
XM_011540050.1:c.6507G=	XP_011538352.1:p.Leu2169=
XM_011540051.1:c.6507G=	XP_011538353.1:p.Leu2169=
XM_011540052.1:c.2835G=	XP_011538354.1:p.Leu945=
XR_945796.1:n.6750G=
NM_022124.6:c.6312G= MANE Select	NP_071407.4:p.Leu2104=