Canonical Allele Identifier: CA470062275

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73560456T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71800699T>C , CM000672.2:g.71800699T>C	GRCh38
NC_000010.10:g.73560456T>C , CM000672.1:g.73560456T>C	GRCh37
NC_000010.9:g.73230462T>C	NCBI36
NG_008835.1:g.408753T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.7426T>C MANE Select	ENSP00000224721.9:p.Leu2476=
ENST00000642965.1:c.1359T>C	ENSP00000495222.1:n.1359T>C
ENST00000647092.1:c.1023T>C	ENSP00000495176.1:n.1023T>C
ENST00000224721.10:c.7441T>C	ENSP00000224721.8:p.Leu2481=
ENST00000398788.4:c.706T>C	ENSP00000381768.3:p.Leu236=
ENST00000475158.1:n.962T>C
ENST00000619887.4:c.706T>C	ENSP00000478374.1:p.Leu236=
ENST00000622827.4:c.7426T>C	ENSP00000483211.1:p.Leu2476=
NM_001171933.1:c.706T>C	NP_001165404.1:p.Leu236=
NM_001171934.1:c.706T>C	NP_001165405.1:p.Leu236=
NM_022124.5:c.7426T>C	NP_071407.4:p.Leu2476=
XM_006717940.2:c.7621T>C	XP_006718003.1:p.Leu2541=
XM_006717942.2:c.7555T>C	XP_006718005.1:p.Leu2519=
XM_011540039.1:c.7618T>C	XP_011538341.1:p.Leu2540=
XM_011540040.1:c.7615T>C	XP_011538342.1:p.Leu2539=
XM_011540041.1:c.7561T>C	XP_011538343.1:p.Leu2521=
XM_011540042.1:c.7531T>C	XP_011538344.1:p.Leu2511=
XM_011540043.1:c.7621T>C	XP_011538345.1:p.Leu2541=
XM_011540044.1:c.7486T>C	XP_011538346.1:p.Leu2496=
XM_011540045.1:c.7621T>C	XP_011538347.1:p.Leu2541=
XM_011540046.1:c.7081T>C	XP_011538348.1:p.Leu2361=
XM_011540047.1:c.6439T>C	XP_011538349.1:p.Leu2147=
XM_011540052.1:c.3949T>C	XP_011538354.1:p.Leu1317=
NM_022124.6:c.7426T>C MANE Select	NP_071407.4:p.Leu2476=