Canonical Allele Identifier: CA377162334

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73565953A>C (hg19) ; chr10:g.71806196A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71806196A>C , CM000672.2:g.71806196A>C	GRCh38
NC_000010.10:g.73565953A>C , CM000672.1:g.73565953A>C	GRCh37
NC_000010.9:g.73235959A>C	NCBI36
NG_008835.1:g.414250A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.8093A>C MANE Select	ENSP00000224721.9:p.Gln2698Pro
ENST00000642965.1:c.2026A>C	ENSP00000495222.1:n.2026A>C
ENST00000647092.1:c.1690A>C	ENSP00000495176.1:n.1690A>C
ENST00000224721.10:c.8108A>C	ENSP00000224721.8:p.Gln2703Pro
ENST00000398788.4:c.1373A>C	ENSP00000381768.3:p.Gln458Pro
ENST00000475158.1:n.1629A>C
ENST00000619887.4:c.1373A>C	ENSP00000478374.1:p.Gln458Pro
ENST00000622827.4:c.8093A>C	ENSP00000483211.1:p.Gln2698Pro
NM_001171933.1:c.1373A>C	NP_001165404.1:p.Gln458Pro
NM_001171934.1:c.1373A>C	NP_001165405.1:p.Gln458Pro
NM_022124.5:c.8093A>C	NP_071407.4:p.Gln2698Pro
XM_006717940.2:c.8288A>C	XP_006718003.1:p.Gln2763Pro
XM_006717942.2:c.8222A>C	XP_006718005.1:p.Gln2741Pro
XM_011540039.1:c.8285A>C	XP_011538341.1:p.Gln2762Pro
XM_011540040.1:c.8282A>C	XP_011538342.1:p.Gln2761Pro
XM_011540041.1:c.8228A>C	XP_011538343.1:p.Gln2743Pro
XM_011540042.1:c.8198A>C	XP_011538344.1:p.Gln2733Pro
XM_011540043.1:c.8288A>C	XP_011538345.1:p.Gln2763Pro
XM_011540044.1:c.8153A>C	XP_011538346.1:p.Gln2718Pro
XM_011540045.1:c.8288A>C	XP_011538347.1:p.Gln2763Pro
XM_011540046.1:c.7748A>C	XP_011538348.1:p.Gln2583Pro
XM_011540047.1:c.7106A>C	XP_011538349.1:p.Gln2369Pro
XM_011540052.1:c.4616A>C	XP_011538354.1:p.Gln1539Pro
NM_022124.6:c.8093A>C MANE Select	NP_071407.4:p.Gln2698Pro