Canonical Allele Identifier: CA377159289

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73559291A>T (hg19) ; chr10:g.71799534A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71799534A>T , CM000672.2:g.71799534A>T	GRCh38
NC_000010.10:g.73559291A>T , CM000672.1:g.73559291A>T	GRCh37
NC_000010.9:g.73229297A>T	NCBI36
NG_008835.1:g.407588A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7267A>T MANE Select	ENSP00000224721.9:p.Thr2423Ser
ENST00000642965.1:c.1200A>T	ENSP00000495222.1:n.1200A>T
ENST00000647092.1:c.864A>T	ENSP00000495176.1:n.864A>T
ENST00000224721.10:c.7282A>T	ENSP00000224721.8:p.Thr2428Ser
ENST00000398788.4:c.547A>T	ENSP00000381768.3:p.Thr183Ser
ENST00000475158.1:n.803A>T
ENST00000619887.4:c.547A>T	ENSP00000478374.1:p.Thr183Ser
ENST00000622827.4:c.7267A>T	ENSP00000483211.1:p.Thr2423Ser
NM_001171933.1:c.547A>T	NP_001165404.1:p.Thr183Ser
NM_001171934.1:c.547A>T	NP_001165405.1:p.Thr183Ser
NM_022124.5:c.7267A>T	NP_071407.4:p.Thr2423Ser
XM_006717940.2:c.7462A>T	XP_006718003.1:p.Thr2488Ser
XM_006717942.2:c.7396A>T	XP_006718005.1:p.Thr2466Ser
XM_011540039.1:c.7459A>T	XP_011538341.1:p.Thr2487Ser
XM_011540040.1:c.7456A>T	XP_011538342.1:p.Thr2486Ser
XM_011540041.1:c.7402A>T	XP_011538343.1:p.Thr2468Ser
XM_011540042.1:c.7372A>T	XP_011538344.1:p.Thr2458Ser
XM_011540043.1:c.7462A>T	XP_011538345.1:p.Thr2488Ser
XM_011540044.1:c.7327A>T	XP_011538346.1:p.Thr2443Ser
XM_011540045.1:c.7462A>T	XP_011538347.1:p.Thr2488Ser
XM_011540046.1:c.6922A>T	XP_011538348.1:p.Thr2308Ser
XM_011540047.1:c.6280A>T	XP_011538349.1:p.Thr2094Ser
XM_011540052.1:c.3790A>T	XP_011538354.1:p.Thr1264Ser
NM_022124.6:c.7267A>T MANE Select	NP_071407.4:p.Thr2423Ser