Canonical Allele Identifier: CA377150551

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73550077C>G (hg19) ; chr10:g.71790320C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71790320C>G , CM000672.2:g.71790320C>G	GRCh38
NC_000010.10:g.73550077C>G , CM000672.1:g.73550077C>G	GRCh37
NC_000010.9:g.73220083C>G	NCBI36
NG_008835.1:g.398374C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.5956C>G MANE Select	ENSP00000224721.9:p.Leu1986Val
ENST00000224721.10:c.5971C>G	ENSP00000224721.8:p.Leu1991Val
ENST00000622827.4:c.5956C>G	ENSP00000483211.1:p.Leu1986Val
NM_022124.5:c.5956C>G	NP_071407.4:p.Leu1986Val
XM_006717940.2:c.6151C>G	XP_006718003.1:p.Leu2051Val
XM_006717942.2:c.6085C>G	XP_006718005.1:p.Leu2029Val
XM_011540039.1:c.6148C>G	XP_011538341.1:p.Leu2050Val
XM_011540040.1:c.6145C>G	XP_011538342.1:p.Leu2049Val
XM_011540041.1:c.6091C>G	XP_011538343.1:p.Leu2031Val
XM_011540042.1:c.6151C>G	XP_011538344.1:p.Leu2051Val
XM_011540043.1:c.6151C>G	XP_011538345.1:p.Leu2051Val
XM_011540044.1:c.6016C>G	XP_011538346.1:p.Leu2006Val
XM_011540045.1:c.6151C>G	XP_011538347.1:p.Leu2051Val
XM_011540046.1:c.5611C>G	XP_011538348.1:p.Leu1871Val
XM_011540047.1:c.4969C>G	XP_011538349.1:p.Leu1657Val
XM_011540048.1:c.6151C>G	XP_011538350.1:p.Leu2051Val
XM_011540049.1:c.6151C>G	XP_011538351.1:p.Leu2051Val
XM_011540050.1:c.6151C>G	XP_011538352.1:p.Leu2051Val
XM_011540051.1:c.6151C>G	XP_011538353.1:p.Leu2051Val
XM_011540052.1:c.2479C>G	XP_011538354.1:p.Leu827Val
XR_945796.1:n.6394C>G
NM_022124.6:c.5956C>G MANE Select	NP_071407.4:p.Leu1986Val