Canonical Allele Identifier: CA209457495

Gene: CDH23

Linked Data

• dbSNP Id: rs577606217
• MyVariant Identifiers: chr10:g.73544722C>T (hg19) ; chr10:g.71784965C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71784965C>T , CM000672.2:g.71784965C>T	GRCh38
NC_000010.10:g.73544722C>T , CM000672.1:g.73544722C>T	GRCh37
NC_000010.9:g.73214728C>T	NCBI36
NG_008835.1:g.393019C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5577C>T MANE Select	ENSP00000224721.9:p.Thr1859=
ENST00000224721.10:c.5592C>T	ENSP00000224721.8:p.Thr1864=
ENST00000622827.4:c.5577C>T	ENSP00000483211.1:p.Thr1859=
NM_022124.5:c.5577C>T	NP_071407.4:p.Thr1859=
XM_006717940.2:c.5772C>T	XP_006718003.1:p.Thr1924=
XM_006717942.2:c.5706C>T	XP_006718005.1:p.Thr1902=
XM_011540039.1:c.5769C>T	XP_011538341.1:p.Thr1923=
XM_011540040.1:c.5766C>T	XP_011538342.1:p.Thr1922=
XM_011540041.1:c.5712C>T	XP_011538343.1:p.Thr1904=
XM_011540042.1:c.5772C>T	XP_011538344.1:p.Thr1924=
XM_011540043.1:c.5772C>T	XP_011538345.1:p.Thr1924=
XM_011540044.1:c.5637C>T	XP_011538346.1:p.Thr1879=
XM_011540045.1:c.5772C>T	XP_011538347.1:p.Thr1924=
XM_011540046.1:c.5232C>T	XP_011538348.1:p.Thr1744=
XM_011540047.1:c.4590C>T	XP_011538349.1:p.Thr1530=
XM_011540048.1:c.5772C>T	XP_011538350.1:p.Thr1924=
XM_011540049.1:c.5772C>T	XP_011538351.1:p.Thr1924=
XM_011540050.1:c.5772C>T	XP_011538352.1:p.Thr1924=
XM_011540051.1:c.5772C>T	XP_011538353.1:p.Thr1924=
XM_011540052.1:c.2100C>T	XP_011538354.1:p.Thr700=
XM_011540053.1:c.5772C>T	XP_011538355.1:p.Thr1924=
XR_945796.1:n.6015C>T
NM_022124.6:c.5577C>T MANE Select	NP_071407.4:p.Thr1859=