Canonical Allele Identifier: CA377146756

Gene: CDH23

Linked Data

• gnomAD v4: 10-71784997-T-C
• MyVariant Identifiers: chr10:g.73544754T>C (hg19) ; chr10:g.71784997T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71784997T>C , CM000672.2:g.71784997T>C	GRCh38
NC_000010.10:g.73544754T>C , CM000672.1:g.73544754T>C	GRCh37
NC_000010.9:g.73214760T>C	NCBI36
NG_008835.1:g.393051T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5609T>C MANE Select	ENSP00000224721.9:p.Val1870Ala
ENST00000224721.10:c.5624T>C	ENSP00000224721.8:p.Val1875Ala
ENST00000622827.4:c.5609T>C	ENSP00000483211.1:p.Val1870Ala
NM_022124.5:c.5609T>C	NP_071407.4:p.Val1870Ala
XM_006717940.2:c.5804T>C	XP_006718003.1:p.Val1935Ala
XM_006717942.2:c.5738T>C	XP_006718005.1:p.Val1913Ala
XM_011540039.1:c.5801T>C	XP_011538341.1:p.Val1934Ala
XM_011540040.1:c.5798T>C	XP_011538342.1:p.Val1933Ala
XM_011540041.1:c.5744T>C	XP_011538343.1:p.Val1915Ala
XM_011540042.1:c.5804T>C	XP_011538344.1:p.Val1935Ala
XM_011540043.1:c.5804T>C	XP_011538345.1:p.Val1935Ala
XM_011540044.1:c.5669T>C	XP_011538346.1:p.Val1890Ala
XM_011540045.1:c.5804T>C	XP_011538347.1:p.Val1935Ala
XM_011540046.1:c.5264T>C	XP_011538348.1:p.Val1755Ala
XM_011540047.1:c.4622T>C	XP_011538349.1:p.Val1541Ala
XM_011540048.1:c.5804T>C	XP_011538350.1:p.Val1935Ala
XM_011540049.1:c.5804T>C	XP_011538351.1:p.Val1935Ala
XM_011540050.1:c.5804T>C	XP_011538352.1:p.Val1935Ala
XM_011540051.1:c.5804T>C	XP_011538353.1:p.Val1935Ala
XM_011540052.1:c.2132T>C	XP_011538354.1:p.Val711Ala
XM_011540053.1:c.5804T>C	XP_011538355.1:p.Val1935Ala
XR_945796.1:n.6047T>C
NM_022124.6:c.5609T>C MANE Select	NP_071407.4:p.Val1870Ala