Canonical Allele Identifier: CA377160935

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73562815T>A (hg19) ; chr10:g.71803058T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71803058T>A , CM000672.2:g.71803058T>A	GRCh38
NC_000010.10:g.73562815T>A , CM000672.1:g.73562815T>A	GRCh37
NC_000010.9:g.73232821T>A	NCBI36
NG_008835.1:g.411112T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7643T>A MANE Select	ENSP00000224721.9:p.Leu2548His
ENST00000642965.1:c.1576T>A	ENSP00000495222.1:n.1576T>A
ENST00000647092.1:c.1240T>A	ENSP00000495176.1:n.1240T>A
ENST00000224721.10:c.7658T>A	ENSP00000224721.8:p.Leu2553His
ENST00000398788.4:c.923T>A	ENSP00000381768.3:p.Leu308His
ENST00000475158.1:n.1179T>A
ENST00000619887.4:c.923T>A	ENSP00000478374.1:p.Leu308His
ENST00000622827.4:c.7643T>A	ENSP00000483211.1:p.Leu2548His
NM_001171933.1:c.923T>A	NP_001165404.1:p.Leu308His
NM_001171934.1:c.923T>A	NP_001165405.1:p.Leu308His
NM_022124.5:c.7643T>A	NP_071407.4:p.Leu2548His
XM_006717940.2:c.7838T>A	XP_006718003.1:p.Leu2613His
XM_006717942.2:c.7772T>A	XP_006718005.1:p.Leu2591His
XM_011540039.1:c.7835T>A	XP_011538341.1:p.Leu2612His
XM_011540040.1:c.7832T>A	XP_011538342.1:p.Leu2611His
XM_011540041.1:c.7778T>A	XP_011538343.1:p.Leu2593His
XM_011540042.1:c.7748T>A	XP_011538344.1:p.Leu2583His
XM_011540043.1:c.7838T>A	XP_011538345.1:p.Leu2613His
XM_011540044.1:c.7703T>A	XP_011538346.1:p.Leu2568His
XM_011540045.1:c.7838T>A	XP_011538347.1:p.Leu2613His
XM_011540046.1:c.7298T>A	XP_011538348.1:p.Leu2433His
XM_011540047.1:c.6656T>A	XP_011538349.1:p.Leu2219His
XM_011540052.1:c.4166T>A	XP_011538354.1:p.Leu1389His
NM_022124.6:c.7643T>A MANE Select	NP_071407.4:p.Leu2548His