Canonical Allele Identifier: CA377153894

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73552950C>G (hg19) ; chr10:g.71793193C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793193C>G , CM000672.2:g.71793193C>G	GRCh38
NC_000010.10:g.73552950C>G , CM000672.1:g.73552950C>G	GRCh37
NC_000010.9:g.73222956C>G	NCBI36
NG_008835.1:g.401247C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6265C>G MANE Select	ENSP00000224721.9:p.Leu2089Val
ENST00000224721.10:c.6280C>G	ENSP00000224721.8:p.Leu2094Val
ENST00000622827.4:c.6265C>G	ENSP00000483211.1:p.Leu2089Val
NM_022124.5:c.6265C>G	NP_071407.4:p.Leu2089Val
XM_006717940.2:c.6460C>G	XP_006718003.1:p.Leu2154Val
XM_006717942.2:c.6394C>G	XP_006718005.1:p.Leu2132Val
XM_011540039.1:c.6457C>G	XP_011538341.1:p.Leu2153Val
XM_011540040.1:c.6454C>G	XP_011538342.1:p.Leu2152Val
XM_011540041.1:c.6400C>G	XP_011538343.1:p.Leu2134Val
XM_011540042.1:c.6460C>G	XP_011538344.1:p.Leu2154Val
XM_011540043.1:c.6460C>G	XP_011538345.1:p.Leu2154Val
XM_011540044.1:c.6325C>G	XP_011538346.1:p.Leu2109Val
XM_011540045.1:c.6460C>G	XP_011538347.1:p.Leu2154Val
XM_011540046.1:c.5920C>G	XP_011538348.1:p.Leu1974Val
XM_011540047.1:c.5278C>G	XP_011538349.1:p.Leu1760Val
XM_011540048.1:c.6460C>G	XP_011538350.1:p.Leu2154Val
XM_011540049.1:c.6460C>G	XP_011538351.1:p.Leu2154Val
XM_011540050.1:c.6460C>G	XP_011538352.1:p.Leu2154Val
XM_011540051.1:c.6460C>G	XP_011538353.1:p.Leu2154Val
XM_011540052.1:c.2788C>G	XP_011538354.1:p.Leu930Val
XR_945796.1:n.6703C>G
NM_022124.6:c.6265C>G MANE Select	NP_071407.4:p.Leu2089Val