Canonical Allele Identifier: CA1918862218

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71784955T= , CM000672.2:g.71784955T=	GRCh38
NC_000010.10:g.73544712T= , CM000672.1:g.73544712T=	GRCh37
NC_000010.9:g.73214718T=	NCBI36
NG_008835.1:g.393009T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5567T= MANE Select	ENSP00000224721.9:p.Met1856=
ENST00000224721.10:c.5582T=	ENSP00000224721.8:p.Met1861=
ENST00000622827.4:c.5567T=	ENSP00000483211.1:p.Met1856=
NM_022124.5:c.5567T=	NP_071407.4:p.Met1856=
XM_006717940.2:c.5762T=	XP_006718003.1:p.Met1921=
XM_006717942.2:c.5696T=	XP_006718005.1:p.Met1899=
XM_011540039.1:c.5759T=	XP_011538341.1:p.Met1920=
XM_011540040.1:c.5756T=	XP_011538342.1:p.Met1919=
XM_011540041.1:c.5702T=	XP_011538343.1:p.Met1901=
XM_011540042.1:c.5762T=	XP_011538344.1:p.Met1921=
XM_011540043.1:c.5762T=	XP_011538345.1:p.Met1921=
XM_011540044.1:c.5627T=	XP_011538346.1:p.Met1876=
XM_011540045.1:c.5762T=	XP_011538347.1:p.Met1921=
XM_011540046.1:c.5222T=	XP_011538348.1:p.Met1741=
XM_011540047.1:c.4580T=	XP_011538349.1:p.Met1527=
XM_011540048.1:c.5762T=	XP_011538350.1:p.Met1921=
XM_011540049.1:c.5762T=	XP_011538351.1:p.Met1921=
XM_011540050.1:c.5762T=	XP_011538352.1:p.Met1921=
XM_011540051.1:c.5762T=	XP_011538353.1:p.Met1921=
XM_011540052.1:c.2090T=	XP_011538354.1:p.Met697=
XM_011540053.1:c.5762T=	XP_011538355.1:p.Met1921=
XR_945796.1:n.6005T=
NM_022124.6:c.5567T= MANE Select	NP_071407.4:p.Met1856=