Canonical Allele Identifier: CA377160760

Gene: CDH23

Linked Data

• gnomAD v4: 10-71740933-A-G
• MyVariant Identifiers: chr10:g.73500690A>G (hg19) ; chr10:g.71740933A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740933A>G , CM000672.2:g.71740933A>G	GRCh38
NC_000010.10:g.73500690A>G , CM000672.1:g.73500690A>G	GRCh37
NC_000010.9:g.73170696A>G	NCBI36
NG_008835.1:g.348987A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4600A>G MANE Select	ENSP00000224721.9:p.Asn1534Asp
ENST00000224721.10:c.4615A>G	ENSP00000224721.8:p.Asn1539Asp
ENST00000398792.3:n.1289A>G
ENST00000622827.4:c.4600A>G	ENSP00000483211.1:p.Asn1534Asp
NM_022124.5:c.4600A>G	NP_071407.4:p.Asn1534Asp
XM_006717940.2:c.4795A>G	XP_006718003.1:p.Asn1599Asp
XM_006717942.2:c.4729A>G	XP_006718005.1:p.Asn1577Asp
XM_011540039.1:c.4792A>G	XP_011538341.1:p.Asn1598Asp
XM_011540040.1:c.4789A>G	XP_011538342.1:p.Asn1597Asp
XM_011540041.1:c.4735A>G	XP_011538343.1:p.Asn1579Asp
XM_011540042.1:c.4795A>G	XP_011538344.1:p.Asn1599Asp
XM_011540043.1:c.4795A>G	XP_011538345.1:p.Asn1599Asp
XM_011540044.1:c.4660A>G	XP_011538346.1:p.Asn1554Asp
XM_011540045.1:c.4795A>G	XP_011538347.1:p.Asn1599Asp
XM_011540046.1:c.4255A>G	XP_011538348.1:p.Asn1419Asp
XM_011540047.1:c.3613A>G	XP_011538349.1:p.Asn1205Asp
XM_011540048.1:c.4795A>G	XP_011538350.1:p.Asn1599Asp
XM_011540049.1:c.4795A>G	XP_011538351.1:p.Asn1599Asp
XM_011540050.1:c.4795A>G	XP_011538352.1:p.Asn1599Asp
XM_011540051.1:c.4795A>G	XP_011538353.1:p.Asn1599Asp
XM_011540052.1:c.1123A>G	XP_011538354.1:p.Asn375Asp
XM_011540053.1:c.4795A>G	XP_011538355.1:p.Asn1599Asp
XR_945796.1:n.5038A>G
NM_022124.6:c.4600A>G MANE Select	NP_071407.4:p.Asn1534Asp