Canonical Allele Identifier: CA377131360

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73567306C>A (hg19) ; chr10:g.71807549C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71807549C>A , CM000672.2:g.71807549C>A	GRCh38
NC_000010.10:g.73567306C>A , CM000672.1:g.73567306C>A	GRCh37
NC_000010.9:g.73237312C>A	NCBI36
NG_008835.1:g.415603C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.8342C>A MANE Select	ENSP00000224721.9:p.Pro2781His
ENST00000642965.1:c.2275C>A	ENSP00000495222.1:n.2275C>A
ENST00000647092.1:c.1939C>A	ENSP00000495176.1:n.1939C>A
ENST00000224721.10:c.8357C>A	ENSP00000224721.8:p.Pro2786His
ENST00000398788.4:c.1622C>A	ENSP00000381768.3:p.Pro541His
ENST00000475158.1:n.1878C>A
ENST00000619887.4:c.1622C>A	ENSP00000478374.1:p.Pro541His
ENST00000622827.4:c.8342C>A	ENSP00000483211.1:p.Pro2781His
NM_001171933.1:c.1622C>A	NP_001165404.1:p.Pro541His
NM_001171934.1:c.1622C>A	NP_001165405.1:p.Pro541His
NM_022124.5:c.8342C>A	NP_071407.4:p.Pro2781His
XM_006717940.2:c.8537C>A	XP_006718003.1:p.Pro2846His
XM_006717942.2:c.8471C>A	XP_006718005.1:p.Pro2824His
XM_011540039.1:c.8534C>A	XP_011538341.1:p.Pro2845His
XM_011540040.1:c.8531C>A	XP_011538342.1:p.Pro2844His
XM_011540041.1:c.8477C>A	XP_011538343.1:p.Pro2826His
XM_011540042.1:c.8447C>A	XP_011538344.1:p.Pro2816His
XM_011540043.1:c.8537C>A	XP_011538345.1:p.Pro2846His
XM_011540044.1:c.8402C>A	XP_011538346.1:p.Pro2801His
XM_011540045.1:c.8537C>A	XP_011538347.1:p.Pro2846His
XM_011540046.1:c.7997C>A	XP_011538348.1:p.Pro2666His
XM_011540047.1:c.7355C>A	XP_011538349.1:p.Pro2452His
XM_011540052.1:c.4865C>A	XP_011538354.1:p.Pro1622His
NM_022124.6:c.8342C>A MANE Select	NP_071407.4:p.Pro2781His