Canonical Allele Identifier: CA377153959

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73552957T>G (hg19) ; chr10:g.71793200T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793200T>G , CM000672.2:g.71793200T>G	GRCh38
NC_000010.10:g.73552957T>G , CM000672.1:g.73552957T>G	GRCh37
NC_000010.9:g.73222963T>G	NCBI36
NG_008835.1:g.401254T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6272T>G MANE Select	ENSP00000224721.9:p.Val2091Gly
ENST00000224721.10:c.6287T>G	ENSP00000224721.8:p.Val2096Gly
ENST00000622827.4:c.6272T>G	ENSP00000483211.1:p.Val2091Gly
NM_022124.5:c.6272T>G	NP_071407.4:p.Val2091Gly
XM_006717940.2:c.6467T>G	XP_006718003.1:p.Val2156Gly
XM_006717942.2:c.6401T>G	XP_006718005.1:p.Val2134Gly
XM_011540039.1:c.6464T>G	XP_011538341.1:p.Val2155Gly
XM_011540040.1:c.6461T>G	XP_011538342.1:p.Val2154Gly
XM_011540041.1:c.6407T>G	XP_011538343.1:p.Val2136Gly
XM_011540042.1:c.6467T>G	XP_011538344.1:p.Val2156Gly
XM_011540043.1:c.6467T>G	XP_011538345.1:p.Val2156Gly
XM_011540044.1:c.6332T>G	XP_011538346.1:p.Val2111Gly
XM_011540045.1:c.6467T>G	XP_011538347.1:p.Val2156Gly
XM_011540046.1:c.5927T>G	XP_011538348.1:p.Val1976Gly
XM_011540047.1:c.5285T>G	XP_011538349.1:p.Val1762Gly
XM_011540048.1:c.6467T>G	XP_011538350.1:p.Val2156Gly
XM_011540049.1:c.6467T>G	XP_011538351.1:p.Val2156Gly
XM_011540050.1:c.6467T>G	XP_011538352.1:p.Val2156Gly
XM_011540051.1:c.6467T>G	XP_011538353.1:p.Val2156Gly
XM_011540052.1:c.2795T>G	XP_011538354.1:p.Val932Gly
XR_945796.1:n.6710T>G
NM_022124.6:c.6272T>G MANE Select	NP_071407.4:p.Val2091Gly