Canonical Allele Identifier: CA377159307

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73559298C>G (hg19) ; chr10:g.71799541C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71799541C>G , CM000672.2:g.71799541C>G	GRCh38
NC_000010.10:g.73559298C>G , CM000672.1:g.73559298C>G	GRCh37
NC_000010.9:g.73229304C>G	NCBI36
NG_008835.1:g.407595C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.7274C>G MANE Select	ENSP00000224721.9:p.Thr2425Ser
ENST00000642965.1:c.1207C>G	ENSP00000495222.1:n.1207C>G
ENST00000647092.1:c.871C>G	ENSP00000495176.1:n.871C>G
ENST00000224721.10:c.7289C>G	ENSP00000224721.8:p.Thr2430Ser
ENST00000398788.4:c.554C>G	ENSP00000381768.3:p.Thr185Ser
ENST00000475158.1:n.810C>G
ENST00000619887.4:c.554C>G	ENSP00000478374.1:p.Thr185Ser
ENST00000622827.4:c.7274C>G	ENSP00000483211.1:p.Thr2425Ser
NM_001171933.1:c.554C>G	NP_001165404.1:p.Thr185Ser
NM_001171934.1:c.554C>G	NP_001165405.1:p.Thr185Ser
NM_022124.5:c.7274C>G	NP_071407.4:p.Thr2425Ser
XM_006717940.2:c.7469C>G	XP_006718003.1:p.Thr2490Ser
XM_006717942.2:c.7403C>G	XP_006718005.1:p.Thr2468Ser
XM_011540039.1:c.7466C>G	XP_011538341.1:p.Thr2489Ser
XM_011540040.1:c.7463C>G	XP_011538342.1:p.Thr2488Ser
XM_011540041.1:c.7409C>G	XP_011538343.1:p.Thr2470Ser
XM_011540042.1:c.7379C>G	XP_011538344.1:p.Thr2460Ser
XM_011540043.1:c.7469C>G	XP_011538345.1:p.Thr2490Ser
XM_011540044.1:c.7334C>G	XP_011538346.1:p.Thr2445Ser
XM_011540045.1:c.7469C>G	XP_011538347.1:p.Thr2490Ser
XM_011540046.1:c.6929C>G	XP_011538348.1:p.Thr2310Ser
XM_011540047.1:c.6287C>G	XP_011538349.1:p.Thr2096Ser
XM_011540052.1:c.3797C>G	XP_011538354.1:p.Thr1266Ser
NM_022124.6:c.7274C>G MANE Select	NP_071407.4:p.Thr2425Ser