Canonical Allele Identifier: CA377155208

Gene: CDH23

Linked Data

• gnomAD v4: 10-71793433-G-A
• MyVariant Identifiers: chr10:g.73553190G>A (hg19) ; chr10:g.71793433G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793433G>A , CM000672.2:g.71793433G>A	GRCh38
NC_000010.10:g.73553190G>A , CM000672.1:g.73553190G>A	GRCh37
NC_000010.9:g.73223196G>A	NCBI36
NG_008835.1:g.401487G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6505G>A MANE Select	ENSP00000224721.9:p.Asp2169Asn
ENST00000224721.10:c.6520G>A	ENSP00000224721.8:p.Asp2174Asn
ENST00000622827.4:c.6505G>A	ENSP00000483211.1:p.Asp2169Asn
NM_022124.5:c.6505G>A	NP_071407.4:p.Asp2169Asn
XM_006717940.2:c.6700G>A	XP_006718003.1:p.Asp2234Asn
XM_006717942.2:c.6634G>A	XP_006718005.1:p.Asp2212Asn
XM_011540039.1:c.6697G>A	XP_011538341.1:p.Asp2233Asn
XM_011540040.1:c.6694G>A	XP_011538342.1:p.Asp2232Asn
XM_011540041.1:c.6640G>A	XP_011538343.1:p.Asp2214Asn
XM_011540042.1:c.6610G>A	XP_011538344.1:p.Asp2204Asn
XM_011540043.1:c.6700G>A	XP_011538345.1:p.Asp2234Asn
XM_011540044.1:c.6565G>A	XP_011538346.1:p.Asp2189Asn
XM_011540045.1:c.6700G>A	XP_011538347.1:p.Asp2234Asn
XM_011540046.1:c.6160G>A	XP_011538348.1:p.Asp2054Asn
XM_011540047.1:c.5518G>A	XP_011538349.1:p.Asp1840Asn
XM_011540048.1:c.6700G>A	XP_011538350.1:p.Asp2234Asn
XM_011540049.1:c.6700G>A	XP_011538351.1:p.Asp2234Asn
XM_011540050.1:c.6700G>A	XP_011538352.1:p.Asp2234Asn
XM_011540051.1:c.6700G>A	XP_011538353.1:p.Asp2234Asn
XM_011540052.1:c.3028G>A	XP_011538354.1:p.Asp1010Asn
XR_945796.1:n.6943G>A
NM_022124.6:c.6505G>A MANE Select	NP_071407.4:p.Asp2169Asn