Canonical Allele Identifier: CA377159409

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73559322A>C (hg19) ; chr10:g.71799565A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71799565A>C , CM000672.2:g.71799565A>C	GRCh38
NC_000010.10:g.73559322A>C , CM000672.1:g.73559322A>C	GRCh37
NC_000010.9:g.73229328A>C	NCBI36
NG_008835.1:g.407619A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7298A>C MANE Select	ENSP00000224721.9:p.Asn2433Thr
ENST00000642965.1:c.1231A>C	ENSP00000495222.1:n.1231A>C
ENST00000647092.1:c.895A>C	ENSP00000495176.1:n.895A>C
ENST00000224721.10:c.7313A>C	ENSP00000224721.8:p.Asn2438Thr
ENST00000398788.4:c.578A>C	ENSP00000381768.3:p.Asn193Thr
ENST00000475158.1:n.834A>C
ENST00000619887.4:c.578A>C	ENSP00000478374.1:p.Asn193Thr
ENST00000622827.4:c.7298A>C	ENSP00000483211.1:p.Asn2433Thr
NM_001171933.1:c.578A>C	NP_001165404.1:p.Asn193Thr
NM_001171934.1:c.578A>C	NP_001165405.1:p.Asn193Thr
NM_022124.5:c.7298A>C	NP_071407.4:p.Asn2433Thr
XM_006717940.2:c.7493A>C	XP_006718003.1:p.Asn2498Thr
XM_006717942.2:c.7427A>C	XP_006718005.1:p.Asn2476Thr
XM_011540039.1:c.7490A>C	XP_011538341.1:p.Asn2497Thr
XM_011540040.1:c.7487A>C	XP_011538342.1:p.Asn2496Thr
XM_011540041.1:c.7433A>C	XP_011538343.1:p.Asn2478Thr
XM_011540042.1:c.7403A>C	XP_011538344.1:p.Asn2468Thr
XM_011540043.1:c.7493A>C	XP_011538345.1:p.Asn2498Thr
XM_011540044.1:c.7358A>C	XP_011538346.1:p.Asn2453Thr
XM_011540045.1:c.7493A>C	XP_011538347.1:p.Asn2498Thr
XM_011540046.1:c.6953A>C	XP_011538348.1:p.Asn2318Thr
XM_011540047.1:c.6311A>C	XP_011538349.1:p.Asn2104Thr
XM_011540052.1:c.3821A>C	XP_011538354.1:p.Asn1274Thr
NM_022124.6:c.7298A>C MANE Select	NP_071407.4:p.Asn2433Thr