Canonical Allele Identifier: CA377146658

Gene: CDH23

Linked Data

• gnomAD v4: 10-71784970-G-A
• MyVariant Identifiers: chr10:g.73544727G>A (hg19) ; chr10:g.71784970G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71784970G>A , CM000672.2:g.71784970G>A	GRCh38
NC_000010.10:g.73544727G>A , CM000672.1:g.73544727G>A	GRCh37
NC_000010.9:g.73214733G>A	NCBI36
NG_008835.1:g.393024G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5582G>A MANE Select	ENSP00000224721.9:p.Ser1861Asn
ENST00000224721.10:c.5597G>A	ENSP00000224721.8:p.Ser1866Asn
ENST00000622827.4:c.5582G>A	ENSP00000483211.1:p.Ser1861Asn
NM_022124.5:c.5582G>A	NP_071407.4:p.Ser1861Asn
XM_006717940.2:c.5777G>A	XP_006718003.1:p.Ser1926Asn
XM_006717942.2:c.5711G>A	XP_006718005.1:p.Ser1904Asn
XM_011540039.1:c.5774G>A	XP_011538341.1:p.Ser1925Asn
XM_011540040.1:c.5771G>A	XP_011538342.1:p.Ser1924Asn
XM_011540041.1:c.5717G>A	XP_011538343.1:p.Ser1906Asn
XM_011540042.1:c.5777G>A	XP_011538344.1:p.Ser1926Asn
XM_011540043.1:c.5777G>A	XP_011538345.1:p.Ser1926Asn
XM_011540044.1:c.5642G>A	XP_011538346.1:p.Ser1881Asn
XM_011540045.1:c.5777G>A	XP_011538347.1:p.Ser1926Asn
XM_011540046.1:c.5237G>A	XP_011538348.1:p.Ser1746Asn
XM_011540047.1:c.4595G>A	XP_011538349.1:p.Ser1532Asn
XM_011540048.1:c.5777G>A	XP_011538350.1:p.Ser1926Asn
XM_011540049.1:c.5777G>A	XP_011538351.1:p.Ser1926Asn
XM_011540050.1:c.5777G>A	XP_011538352.1:p.Ser1926Asn
XM_011540051.1:c.5777G>A	XP_011538353.1:p.Ser1926Asn
XM_011540052.1:c.2105G>A	XP_011538354.1:p.Ser702Asn
XM_011540053.1:c.5777G>A	XP_011538355.1:p.Ser1926Asn
XR_945796.1:n.6020G>A
NM_022124.6:c.5582G>A MANE Select	NP_071407.4:p.Ser1861Asn