Canonical Allele Identifier: CA377131484

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73567372T>C (hg19) ; chr10:g.71807615T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71807615T>C , CM000672.2:g.71807615T>C	GRCh38
NC_000010.10:g.73567372T>C , CM000672.1:g.73567372T>C	GRCh37
NC_000010.9:g.73237378T>C	NCBI36
NG_008835.1:g.415669T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.8408T>C MANE Select	ENSP00000224721.9:p.Val2803Ala
ENST00000642965.1:c.2341T>C	ENSP00000495222.1:n.2341T>C
ENST00000647092.1:c.2005T>C	ENSP00000495176.1:n.2005T>C
ENST00000224721.10:c.8423T>C	ENSP00000224721.8:p.Val2808Ala
ENST00000398788.4:c.1688T>C	ENSP00000381768.3:p.Val563Ala
ENST00000475158.1:n.1944T>C
ENST00000619887.4:c.1688T>C	ENSP00000478374.1:p.Val563Ala
ENST00000622827.4:c.8408T>C	ENSP00000483211.1:p.Val2803Ala
NM_001171933.1:c.1688T>C	NP_001165404.1:p.Val563Ala
NM_001171934.1:c.1688T>C	NP_001165405.1:p.Val563Ala
NM_022124.5:c.8408T>C	NP_071407.4:p.Val2803Ala
XM_006717940.2:c.8603T>C	XP_006718003.1:p.Val2868Ala
XM_006717942.2:c.8537T>C	XP_006718005.1:p.Val2846Ala
XM_011540039.1:c.8600T>C	XP_011538341.1:p.Val2867Ala
XM_011540040.1:c.8597T>C	XP_011538342.1:p.Val2866Ala
XM_011540041.1:c.8543T>C	XP_011538343.1:p.Val2848Ala
XM_011540042.1:c.8513T>C	XP_011538344.1:p.Val2838Ala
XM_011540043.1:c.8603T>C	XP_011538345.1:p.Val2868Ala
XM_011540044.1:c.8468T>C	XP_011538346.1:p.Val2823Ala
XM_011540045.1:c.8603T>C	XP_011538347.1:p.Val2868Ala
XM_011540046.1:c.8063T>C	XP_011538348.1:p.Val2688Ala
XM_011540047.1:c.7421T>C	XP_011538349.1:p.Val2474Ala
XM_011540052.1:c.4931T>C	XP_011538354.1:p.Val1644Ala
NM_022124.6:c.8408T>C MANE Select	NP_071407.4:p.Val2803Ala