Canonical Allele Identifier: CA470069233

Gene: CDH23

Linked Data

• dbSNP Id: rs1275125853
• gnomAD v3: 10-71740899-C-T
• gnomAD v4: 10-71740899-C-T
• MyVariant Identifiers: chr10:g.73500656C>T (hg19) ; chr10:g.71740899C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740899C>T , CM000672.2:g.71740899C>T	GRCh38
NC_000010.10:g.73500656C>T , CM000672.1:g.73500656C>T	GRCh37
NC_000010.9:g.73170662C>T	NCBI36
NG_008835.1:g.348953C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4566C>T MANE Select	ENSP00000224721.9:p.Asp1522=
ENST00000224721.10:c.4581C>T	ENSP00000224721.8:p.Asp1527=
ENST00000398792.3:n.1255C>T
ENST00000622827.4:c.4566C>T	ENSP00000483211.1:p.Asp1522=
NM_022124.5:c.4566C>T	NP_071407.4:p.Asp1522=
XM_006717940.2:c.4761C>T	XP_006718003.1:p.Asp1587=
XM_006717942.2:c.4695C>T	XP_006718005.1:p.Asp1565=
XM_011540039.1:c.4758C>T	XP_011538341.1:p.Asp1586=
XM_011540040.1:c.4755C>T	XP_011538342.1:p.Asp1585=
XM_011540041.1:c.4701C>T	XP_011538343.1:p.Asp1567=
XM_011540042.1:c.4761C>T	XP_011538344.1:p.Asp1587=
XM_011540043.1:c.4761C>T	XP_011538345.1:p.Asp1587=
XM_011540044.1:c.4626C>T	XP_011538346.1:p.Asp1542=
XM_011540045.1:c.4761C>T	XP_011538347.1:p.Asp1587=
XM_011540046.1:c.4221C>T	XP_011538348.1:p.Asp1407=
XM_011540047.1:c.3579C>T	XP_011538349.1:p.Asp1193=
XM_011540048.1:c.4761C>T	XP_011538350.1:p.Asp1587=
XM_011540049.1:c.4761C>T	XP_011538351.1:p.Asp1587=
XM_011540050.1:c.4761C>T	XP_011538352.1:p.Asp1587=
XM_011540051.1:c.4761C>T	XP_011538353.1:p.Asp1587=
XM_011540052.1:c.1089C>T	XP_011538354.1:p.Asp363=
XM_011540053.1:c.4761C>T	XP_011538355.1:p.Asp1587=
XR_945796.1:n.5004C>T
NM_022124.6:c.4566C>T MANE Select	NP_071407.4:p.Asp1522=