Canonical Allele Identifier: CA377155202

Gene: CDH23

Linked Data

• dbSNP Id: rs1433013026
• gnomAD v2: 10-73553187-A-G
• gnomAD v3: 10-71793430-A-G
• gnomAD v4: 10-71793430-A-G
• MyVariant Identifiers: chr10:g.73553187A>G (hg19) ; chr10:g.71793430A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793430A>G , CM000672.2:g.71793430A>G	GRCh38
NC_000010.10:g.73553187A>G , CM000672.1:g.73553187A>G	GRCh37
NC_000010.9:g.73223193A>G	NCBI36
NG_008835.1:g.401484A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6502A>G MANE Select	ENSP00000224721.9:p.Asn2168Asp
ENST00000224721.10:c.6517A>G	ENSP00000224721.8:p.Asn2173Asp
ENST00000622827.4:c.6502A>G	ENSP00000483211.1:p.Asn2168Asp
NM_022124.5:c.6502A>G	NP_071407.4:p.Asn2168Asp
XM_006717940.2:c.6697A>G	XP_006718003.1:p.Asn2233Asp
XM_006717942.2:c.6631A>G	XP_006718005.1:p.Asn2211Asp
XM_011540039.1:c.6694A>G	XP_011538341.1:p.Asn2232Asp
XM_011540040.1:c.6691A>G	XP_011538342.1:p.Asn2231Asp
XM_011540041.1:c.6637A>G	XP_011538343.1:p.Asn2213Asp
XM_011540042.1:c.6607A>G	XP_011538344.1:p.Asn2203Asp
XM_011540043.1:c.6697A>G	XP_011538345.1:p.Asn2233Asp
XM_011540044.1:c.6562A>G	XP_011538346.1:p.Asn2188Asp
XM_011540045.1:c.6697A>G	XP_011538347.1:p.Asn2233Asp
XM_011540046.1:c.6157A>G	XP_011538348.1:p.Asn2053Asp
XM_011540047.1:c.5515A>G	XP_011538349.1:p.Asn1839Asp
XM_011540048.1:c.6697A>G	XP_011538350.1:p.Asn2233Asp
XM_011540049.1:c.6697A>G	XP_011538351.1:p.Asn2233Asp
XM_011540050.1:c.6697A>G	XP_011538352.1:p.Asn2233Asp
XM_011540051.1:c.6697A>G	XP_011538353.1:p.Asn2233Asp
XM_011540052.1:c.3025A>G	XP_011538354.1:p.Asn1009Asp
XR_945796.1:n.6940A>G
NM_022124.6:c.6502A>G MANE Select	NP_071407.4:p.Asn2168Asp