Canonical Allele Identifier: CA377131566

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73567414C>A (hg19) ; chr10:g.71807657C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71807657C>A , CM000672.2:g.71807657C>A	GRCh38
NC_000010.10:g.73567414C>A , CM000672.1:g.73567414C>A	GRCh37
NC_000010.9:g.73237420C>A	NCBI36
NG_008835.1:g.415711C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.8450C>A MANE Select	ENSP00000224721.9:p.Pro2817His
ENST00000642965.1:c.2383C>A	ENSP00000495222.1:n.2383C>A
ENST00000647092.1:c.2047C>A	ENSP00000495176.1:n.2047C>A
ENST00000224721.10:c.8465C>A	ENSP00000224721.8:p.Pro2822His
ENST00000398788.4:c.1730C>A	ENSP00000381768.3:p.Pro577His
ENST00000475158.1:n.1986C>A
ENST00000619887.4:c.1730C>A	ENSP00000478374.1:p.Pro577His
ENST00000622827.4:c.8450C>A	ENSP00000483211.1:p.Pro2817His
NM_001171933.1:c.1730C>A	NP_001165404.1:p.Pro577His
NM_001171934.1:c.1730C>A	NP_001165405.1:p.Pro577His
NM_022124.5:c.8450C>A	NP_071407.4:p.Pro2817His
XM_006717940.2:c.8645C>A	XP_006718003.1:p.Pro2882His
XM_006717942.2:c.8579C>A	XP_006718005.1:p.Pro2860His
XM_011540039.1:c.8642C>A	XP_011538341.1:p.Pro2881His
XM_011540040.1:c.8639C>A	XP_011538342.1:p.Pro2880His
XM_011540041.1:c.8585C>A	XP_011538343.1:p.Pro2862His
XM_011540042.1:c.8555C>A	XP_011538344.1:p.Pro2852His
XM_011540043.1:c.8645C>A	XP_011538345.1:p.Pro2882His
XM_011540044.1:c.8510C>A	XP_011538346.1:p.Pro2837His
XM_011540045.1:c.8645C>A	XP_011538347.1:p.Pro2882His
XM_011540046.1:c.8105C>A	XP_011538348.1:p.Pro2702His
XM_011540047.1:c.7463C>A	XP_011538349.1:p.Pro2488His
XM_011540052.1:c.4973C>A	XP_011538354.1:p.Pro1658His
NM_022124.6:c.8450C>A MANE Select	NP_071407.4:p.Pro2817His