Canonical Allele Identifier: CA377146806

Gene: CDH23

Linked Data

• dbSNP Id: rs2132939319
• MyVariant Identifiers: chr10:g.73544769C>T (hg19) ; chr10:g.71785012C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71785012C>T , CM000672.2:g.71785012C>T	GRCh38
NC_000010.10:g.73544769C>T , CM000672.1:g.73544769C>T	GRCh37
NC_000010.9:g.73214775C>T	NCBI36
NG_008835.1:g.393066C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.5624C>T MANE Select	ENSP00000224721.9:p.Ala1875Val
ENST00000224721.10:c.5639C>T	ENSP00000224721.8:p.Ala1880Val
ENST00000622827.4:c.5624C>T	ENSP00000483211.1:p.Ala1875Val
NM_022124.5:c.5624C>T	NP_071407.4:p.Ala1875Val
XM_006717940.2:c.5819C>T	XP_006718003.1:p.Ala1940Val
XM_006717942.2:c.5753C>T	XP_006718005.1:p.Ala1918Val
XM_011540039.1:c.5816C>T	XP_011538341.1:p.Ala1939Val
XM_011540040.1:c.5813C>T	XP_011538342.1:p.Ala1938Val
XM_011540041.1:c.5759C>T	XP_011538343.1:p.Ala1920Val
XM_011540042.1:c.5819C>T	XP_011538344.1:p.Ala1940Val
XM_011540043.1:c.5819C>T	XP_011538345.1:p.Ala1940Val
XM_011540044.1:c.5684C>T	XP_011538346.1:p.Ala1895Val
XM_011540045.1:c.5819C>T	XP_011538347.1:p.Ala1940Val
XM_011540046.1:c.5279C>T	XP_011538348.1:p.Ala1760Val
XM_011540047.1:c.4637C>T	XP_011538349.1:p.Ala1546Val
XM_011540048.1:c.5819C>T	XP_011538350.1:p.Ala1940Val
XM_011540049.1:c.5819C>T	XP_011538351.1:p.Ala1940Val
XM_011540050.1:c.5819C>T	XP_011538352.1:p.Ala1940Val
XM_011540051.1:c.5819C>T	XP_011538353.1:p.Ala1940Val
XM_011540052.1:c.2147C>T	XP_011538354.1:p.Ala716Val
XM_011540053.1:c.5819C>T	XP_011538355.1:p.Ala1940Val
XR_945796.1:n.6062C>T
NM_022124.6:c.5624C>T MANE Select	NP_071407.4:p.Ala1875Val