Canonical Allele Identifier: CA377131292

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73567278A>T (hg19) ; chr10:g.71807521A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71807521A>T , CM000672.2:g.71807521A>T	GRCh38
NC_000010.10:g.73567278A>T , CM000672.1:g.73567278A>T	GRCh37
NC_000010.9:g.73237284A>T	NCBI36
NG_008835.1:g.415575A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.8314A>T MANE Select	ENSP00000224721.9:p.Asn2772Tyr
ENST00000642965.1:c.2247A>T	ENSP00000495222.1:n.2247A>T
ENST00000647092.1:c.1911A>T	ENSP00000495176.1:n.1911A>T
ENST00000224721.10:c.8329A>T	ENSP00000224721.8:p.Asn2777Tyr
ENST00000398788.4:c.1594A>T	ENSP00000381768.3:p.Asn532Tyr
ENST00000475158.1:n.1850A>T
ENST00000619887.4:c.1594A>T	ENSP00000478374.1:p.Asn532Tyr
ENST00000622827.4:c.8314A>T	ENSP00000483211.1:p.Asn2772Tyr
NM_001171933.1:c.1594A>T	NP_001165404.1:p.Asn532Tyr
NM_001171934.1:c.1594A>T	NP_001165405.1:p.Asn532Tyr
NM_022124.5:c.8314A>T	NP_071407.4:p.Asn2772Tyr
XM_006717940.2:c.8509A>T	XP_006718003.1:p.Asn2837Tyr
XM_006717942.2:c.8443A>T	XP_006718005.1:p.Asn2815Tyr
XM_011540039.1:c.8506A>T	XP_011538341.1:p.Asn2836Tyr
XM_011540040.1:c.8503A>T	XP_011538342.1:p.Asn2835Tyr
XM_011540041.1:c.8449A>T	XP_011538343.1:p.Asn2817Tyr
XM_011540042.1:c.8419A>T	XP_011538344.1:p.Asn2807Tyr
XM_011540043.1:c.8509A>T	XP_011538345.1:p.Asn2837Tyr
XM_011540044.1:c.8374A>T	XP_011538346.1:p.Asn2792Tyr
XM_011540045.1:c.8509A>T	XP_011538347.1:p.Asn2837Tyr
XM_011540046.1:c.7969A>T	XP_011538348.1:p.Asn2657Tyr
XM_011540047.1:c.7327A>T	XP_011538349.1:p.Asn2443Tyr
XM_011540052.1:c.4837A>T	XP_011538354.1:p.Asn1613Tyr
NM_022124.6:c.8314A>T MANE Select	NP_071407.4:p.Asn2772Tyr