Canonical Allele Identifier: CA470061400

Gene: CDH23

Linked Data

• dbSNP Id: rs1383039387
• MyVariant Identifiers: chr10:g.73550083C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71790326C>T , CM000672.2:g.71790326C>T	GRCh38
NC_000010.10:g.73550083C>T , CM000672.1:g.73550083C>T	GRCh37
NC_000010.9:g.73220089C>T	NCBI36
NG_008835.1:g.398380C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.5962C>T MANE Select	ENSP00000224721.9:p.Leu1988=
ENST00000224721.10:c.5977C>T	ENSP00000224721.8:p.Leu1993=
ENST00000622827.4:c.5962C>T	ENSP00000483211.1:p.Leu1988=
NM_022124.5:c.5962C>T	NP_071407.4:p.Leu1988=
XM_006717940.2:c.6157C>T	XP_006718003.1:p.Leu2053=
XM_006717942.2:c.6091C>T	XP_006718005.1:p.Leu2031=
XM_011540039.1:c.6154C>T	XP_011538341.1:p.Leu2052=
XM_011540040.1:c.6151C>T	XP_011538342.1:p.Leu2051=
XM_011540041.1:c.6097C>T	XP_011538343.1:p.Leu2033=
XM_011540042.1:c.6157C>T	XP_011538344.1:p.Leu2053=
XM_011540043.1:c.6157C>T	XP_011538345.1:p.Leu2053=
XM_011540044.1:c.6022C>T	XP_011538346.1:p.Leu2008=
XM_011540045.1:c.6157C>T	XP_011538347.1:p.Leu2053=
XM_011540046.1:c.5617C>T	XP_011538348.1:p.Leu1873=
XM_011540047.1:c.4975C>T	XP_011538349.1:p.Leu1659=
XM_011540048.1:c.6157C>T	XP_011538350.1:p.Leu2053=
XM_011540049.1:c.6157C>T	XP_011538351.1:p.Leu2053=
XM_011540050.1:c.6157C>T	XP_011538352.1:p.Leu2053=
XM_011540051.1:c.6157C>T	XP_011538353.1:p.Leu2053=
XM_011540052.1:c.2485C>T	XP_011538354.1:p.Leu829=
XR_945796.1:n.6400C>T
NM_022124.6:c.5962C>T MANE Select	NP_071407.4:p.Leu1988=