Canonical Allele Identifier: CA377131488

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73567375A>T (hg19) ; chr10:g.71807618A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71807618A>T , CM000672.2:g.71807618A>T	GRCh38
NC_000010.10:g.73567375A>T , CM000672.1:g.73567375A>T	GRCh37
NC_000010.9:g.73237381A>T	NCBI36
NG_008835.1:g.415672A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.8411A>T MANE Select	ENSP00000224721.9:p.Lys2804Met
ENST00000642965.1:c.2344A>T	ENSP00000495222.1:n.2344A>T
ENST00000647092.1:c.2008A>T	ENSP00000495176.1:n.2008A>T
ENST00000224721.10:c.8426A>T	ENSP00000224721.8:p.Lys2809Met
ENST00000398788.4:c.1691A>T	ENSP00000381768.3:p.Lys564Met
ENST00000475158.1:n.1947A>T
ENST00000619887.4:c.1691A>T	ENSP00000478374.1:p.Lys564Met
ENST00000622827.4:c.8411A>T	ENSP00000483211.1:p.Lys2804Met
NM_001171933.1:c.1691A>T	NP_001165404.1:p.Lys564Met
NM_001171934.1:c.1691A>T	NP_001165405.1:p.Lys564Met
NM_022124.5:c.8411A>T	NP_071407.4:p.Lys2804Met
XM_006717940.2:c.8606A>T	XP_006718003.1:p.Lys2869Met
XM_006717942.2:c.8540A>T	XP_006718005.1:p.Lys2847Met
XM_011540039.1:c.8603A>T	XP_011538341.1:p.Lys2868Met
XM_011540040.1:c.8600A>T	XP_011538342.1:p.Lys2867Met
XM_011540041.1:c.8546A>T	XP_011538343.1:p.Lys2849Met
XM_011540042.1:c.8516A>T	XP_011538344.1:p.Lys2839Met
XM_011540043.1:c.8606A>T	XP_011538345.1:p.Lys2869Met
XM_011540044.1:c.8471A>T	XP_011538346.1:p.Lys2824Met
XM_011540045.1:c.8606A>T	XP_011538347.1:p.Lys2869Met
XM_011540046.1:c.8066A>T	XP_011538348.1:p.Lys2689Met
XM_011540047.1:c.7424A>T	XP_011538349.1:p.Lys2475Met
XM_011540052.1:c.4934A>T	XP_011538354.1:p.Lys1645Met
NM_022124.6:c.8411A>T MANE Select	NP_071407.4:p.Lys2804Met