Canonical Allele Identifier: CA377131584

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73567423C>G (hg19) ; chr10:g.71807666C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71807666C>G , CM000672.2:g.71807666C>G	GRCh38
NC_000010.10:g.73567423C>G , CM000672.1:g.73567423C>G	GRCh37
NC_000010.9:g.73237429C>G	NCBI36
NG_008835.1:g.415720C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.8459C>G MANE Select	ENSP00000224721.9:p.Thr2820Ser
ENST00000642965.1:c.2392C>G	ENSP00000495222.1:n.2392C>G
ENST00000647092.1:c.2056C>G	ENSP00000495176.1:n.2056C>G
ENST00000224721.10:c.8474C>G	ENSP00000224721.8:p.Thr2825Ser
ENST00000398788.4:c.1739C>G	ENSP00000381768.3:p.Thr580Ser
ENST00000475158.1:n.1995C>G
ENST00000619887.4:c.1739C>G	ENSP00000478374.1:p.Thr580Ser
ENST00000622827.4:c.8459C>G	ENSP00000483211.1:p.Thr2820Ser
NM_001171933.1:c.1739C>G	NP_001165404.1:p.Thr580Ser
NM_001171934.1:c.1739C>G	NP_001165405.1:p.Thr580Ser
NM_022124.5:c.8459C>G	NP_071407.4:p.Thr2820Ser
XM_006717940.2:c.8654C>G	XP_006718003.1:p.Thr2885Ser
XM_006717942.2:c.8588C>G	XP_006718005.1:p.Thr2863Ser
XM_011540039.1:c.8651C>G	XP_011538341.1:p.Thr2884Ser
XM_011540040.1:c.8648C>G	XP_011538342.1:p.Thr2883Ser
XM_011540041.1:c.8594C>G	XP_011538343.1:p.Thr2865Ser
XM_011540042.1:c.8564C>G	XP_011538344.1:p.Thr2855Ser
XM_011540043.1:c.8654C>G	XP_011538345.1:p.Thr2885Ser
XM_011540044.1:c.8519C>G	XP_011538346.1:p.Thr2840Ser
XM_011540045.1:c.8654C>G	XP_011538347.1:p.Thr2885Ser
XM_011540046.1:c.8114C>G	XP_011538348.1:p.Thr2705Ser
XM_011540047.1:c.7472C>G	XP_011538349.1:p.Thr2491Ser
XM_011540052.1:c.4982C>G	XP_011538354.1:p.Thr1661Ser
NM_022124.6:c.8459C>G MANE Select	NP_071407.4:p.Thr2820Ser