Canonical Allele Identifier: CA137649

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71815086G>A , CM000672.2:g.71815086G>A	GRCh38
NC_000010.10:g.73574843G>A , CM000672.1:g.73574843G>A	GRCh37
NC_000010.9:g.73244849G>A	NCBI36
NG_008835.1:g.423140G>A
NG_009301.1:g.41240C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.9873G>A MANE Select	ENSP00000224721.9:p.Thr3291=
ENST00000642965.1:c.3806G>A	ENSP00000495222.1:n.3806G>A
ENST00000647092.1:c.3365G>A	ENSP00000495176.1:n.3365G>A
ENST00000224721.10:c.9888G>A	ENSP00000224721.8:p.Thr3296=
ENST00000398788.4:c.3153G>A	ENSP00000381768.3:p.Thr1051=
ENST00000475158.1:n.3304G>A
ENST00000619887.4:c.3048G>A	ENSP00000478374.1:p.Thr1016=
ENST00000622827.4:c.9873G>A	ENSP00000483211.1:p.Thr3291=
NM_001171933.1:c.3153G>A	NP_001165404.1:p.Thr1051=
NM_001171934.1:c.3048G>A	NP_001165405.1:p.Thr1016=
NM_001171935.1:c.564G>A	NP_001165406.1:p.Thr188=
NM_001171936.1:c.459G>A	NP_001165407.1:p.Thr153=
NM_022124.5:c.9873G>A	NP_071407.4:p.Thr3291=
XM_006717940.2:c.10068G>A	XP_006718003.1:p.Thr3356=
XM_006717942.2:c.10002G>A	XP_006718005.1:p.Thr3334=
XM_011540039.1:c.10065G>A	XP_011538341.1:p.Thr3355=
XM_011540040.1:c.10062G>A	XP_011538342.1:p.Thr3354=
XM_011540041.1:c.10008G>A	XP_011538343.1:p.Thr3336=
XM_011540042.1:c.9978G>A	XP_011538344.1:p.Thr3326=
XM_011540043.1:c.9963G>A	XP_011538345.1:p.Thr3321=
XM_011540044.1:c.9933G>A	XP_011538346.1:p.Thr3311=
XM_011540046.1:c.9528G>A	XP_011538348.1:p.Thr3176=
XM_011540047.1:c.8886G>A	XP_011538349.1:p.Thr2962=
XM_011540052.1:c.6396G>A	XP_011538354.1:p.Thr2132=
NM_022124.6:c.9873G>A MANE Select	NP_071407.4:p.Thr3291=