Canonical Allele Identifier: CA377131289

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73567276G>T (hg19) ; chr10:g.71807519G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71807519G>T , CM000672.2:g.71807519G>T	GRCh38
NC_000010.10:g.73567276G>T , CM000672.1:g.73567276G>T	GRCh37
NC_000010.9:g.73237282G>T	NCBI36
NG_008835.1:g.415573G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.8312G>T MANE Select	ENSP00000224721.9:p.Gly2771Val
ENST00000642965.1:c.2245G>T	ENSP00000495222.1:n.2245G>T
ENST00000647092.1:c.1909G>T	ENSP00000495176.1:n.1909G>T
ENST00000224721.10:c.8327G>T	ENSP00000224721.8:p.Gly2776Val
ENST00000398788.4:c.1592G>T	ENSP00000381768.3:p.Gly531Val
ENST00000475158.1:n.1848G>T
ENST00000619887.4:c.1592G>T	ENSP00000478374.1:p.Gly531Val
ENST00000622827.4:c.8312G>T	ENSP00000483211.1:p.Gly2771Val
NM_001171933.1:c.1592G>T	NP_001165404.1:p.Gly531Val
NM_001171934.1:c.1592G>T	NP_001165405.1:p.Gly531Val
NM_022124.5:c.8312G>T	NP_071407.4:p.Gly2771Val
XM_006717940.2:c.8507G>T	XP_006718003.1:p.Gly2836Val
XM_006717942.2:c.8441G>T	XP_006718005.1:p.Gly2814Val
XM_011540039.1:c.8504G>T	XP_011538341.1:p.Gly2835Val
XM_011540040.1:c.8501G>T	XP_011538342.1:p.Gly2834Val
XM_011540041.1:c.8447G>T	XP_011538343.1:p.Gly2816Val
XM_011540042.1:c.8417G>T	XP_011538344.1:p.Gly2806Val
XM_011540043.1:c.8507G>T	XP_011538345.1:p.Gly2836Val
XM_011540044.1:c.8372G>T	XP_011538346.1:p.Gly2791Val
XM_011540045.1:c.8507G>T	XP_011538347.1:p.Gly2836Val
XM_011540046.1:c.7967G>T	XP_011538348.1:p.Gly2656Val
XM_011540047.1:c.7325G>T	XP_011538349.1:p.Gly2442Val
XM_011540052.1:c.4835G>T	XP_011538354.1:p.Gly1612Val
NM_022124.6:c.8312G>T MANE Select	NP_071407.4:p.Gly2771Val