Canonical Allele Identifier: CA377133114

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73569627C>G (hg19) ; chr10:g.71809870C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71809870C>G , CM000672.2:g.71809870C>G	GRCh38
NC_000010.10:g.73569627C>G , CM000672.1:g.73569627C>G	GRCh37
NC_000010.9:g.73239633C>G	NCBI36
NG_008835.1:g.417924C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.8773C>G MANE Select	ENSP00000224721.9:p.Pro2925Ala
ENST00000642965.1:c.2706C>G	ENSP00000495222.1:n.2706C>G
ENST00000647092.1:c.2370C>G	ENSP00000495176.1:n.2370C>G
ENST00000224721.10:c.8788C>G	ENSP00000224721.8:p.Pro2930Ala
ENST00000398788.4:c.2053C>G	ENSP00000381768.3:p.Pro685Ala
ENST00000475158.1:n.2309C>G
ENST00000619887.4:c.2053C>G	ENSP00000478374.1:p.Pro685Ala
ENST00000622827.4:c.8773C>G	ENSP00000483211.1:p.Pro2925Ala
NM_001171933.1:c.2053C>G	NP_001165404.1:p.Pro685Ala
NM_001171934.1:c.2053C>G	NP_001165405.1:p.Pro685Ala
NM_022124.5:c.8773C>G	NP_071407.4:p.Pro2925Ala
XM_006717940.2:c.8968C>G	XP_006718003.1:p.Pro2990Ala
XM_006717942.2:c.8902C>G	XP_006718005.1:p.Pro2968Ala
XM_011540039.1:c.8965C>G	XP_011538341.1:p.Pro2989Ala
XM_011540040.1:c.8962C>G	XP_011538342.1:p.Pro2988Ala
XM_011540041.1:c.8908C>G	XP_011538343.1:p.Pro2970Ala
XM_011540042.1:c.8878C>G	XP_011538344.1:p.Pro2960Ala
XM_011540043.1:c.8968C>G	XP_011538345.1:p.Pro2990Ala
XM_011540044.1:c.8833C>G	XP_011538346.1:p.Pro2945Ala
XM_011540045.1:c.8968C>G	XP_011538347.1:p.Pro2990Ala
XM_011540046.1:c.8428C>G	XP_011538348.1:p.Pro2810Ala
XM_011540047.1:c.7786C>G	XP_011538349.1:p.Pro2596Ala
XM_011540052.1:c.5296C>G	XP_011538354.1:p.Pro1766Ala
NM_022124.6:c.8773C>G MANE Select	NP_071407.4:p.Pro2925Ala