Canonical Allele Identifier: CA377154082

Gene: CDH23

Linked Data

• gnomAD v4: 10-71793219-C-G
• MyVariant Identifiers: chr10:g.73552976C>G (hg19) ; chr10:g.71793219C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793219C>G , CM000672.2:g.71793219C>G	GRCh38
NC_000010.10:g.73552976C>G , CM000672.1:g.73552976C>G	GRCh37
NC_000010.9:g.73222982C>G	NCBI36
NG_008835.1:g.401273C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6291C>G MANE Select	ENSP00000224721.9:p.Asp2097Glu
ENST00000224721.10:c.6306C>G	ENSP00000224721.8:p.Asp2102Glu
ENST00000622827.4:c.6291C>G	ENSP00000483211.1:p.Asp2097Glu
NM_022124.5:c.6291C>G	NP_071407.4:p.Asp2097Glu
XM_006717940.2:c.6486C>G	XP_006718003.1:p.Asp2162Glu
XM_006717942.2:c.6420C>G	XP_006718005.1:p.Asp2140Glu
XM_011540039.1:c.6483C>G	XP_011538341.1:p.Asp2161Glu
XM_011540040.1:c.6480C>G	XP_011538342.1:p.Asp2160Glu
XM_011540041.1:c.6426C>G	XP_011538343.1:p.Asp2142Glu
XM_011540042.1:c.6486C>G	XP_011538344.1:p.Asp2162Glu
XM_011540043.1:c.6486C>G	XP_011538345.1:p.Asp2162Glu
XM_011540044.1:c.6351C>G	XP_011538346.1:p.Asp2117Glu
XM_011540045.1:c.6486C>G	XP_011538347.1:p.Asp2162Glu
XM_011540046.1:c.5946C>G	XP_011538348.1:p.Asp1982Glu
XM_011540047.1:c.5304C>G	XP_011538349.1:p.Asp1768Glu
XM_011540048.1:c.6486C>G	XP_011538350.1:p.Asp2162Glu
XM_011540049.1:c.6486C>G	XP_011538351.1:p.Asp2162Glu
XM_011540050.1:c.6486C>G	XP_011538352.1:p.Asp2162Glu
XM_011540051.1:c.6486C>G	XP_011538353.1:p.Asp2162Glu
XM_011540052.1:c.2814C>G	XP_011538354.1:p.Asp938Glu
XR_945796.1:n.6729C>G
NM_022124.6:c.6291C>G MANE Select	NP_071407.4:p.Asp2097Glu