Canonical Allele Identifier: CA377160641

Gene: CDH23

Linked Data

• dbSNP Id: rs2132846278
• MyVariant Identifiers: chr10:g.73500664C>G (hg19) ; chr10:g.71740907C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740907C>G , CM000672.2:g.71740907C>G	GRCh38
NC_000010.10:g.73500664C>G , CM000672.1:g.73500664C>G	GRCh37
NC_000010.9:g.73170670C>G	NCBI36
NG_008835.1:g.348961C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4574C>G MANE Select	ENSP00000224721.9:p.Pro1525Arg
ENST00000224721.10:c.4589C>G	ENSP00000224721.8:p.Pro1530Arg
ENST00000398792.3:n.1263C>G
ENST00000622827.4:c.4574C>G	ENSP00000483211.1:p.Pro1525Arg
NM_022124.5:c.4574C>G	NP_071407.4:p.Pro1525Arg
XM_006717940.2:c.4769C>G	XP_006718003.1:p.Pro1590Arg
XM_006717942.2:c.4703C>G	XP_006718005.1:p.Pro1568Arg
XM_011540039.1:c.4766C>G	XP_011538341.1:p.Pro1589Arg
XM_011540040.1:c.4763C>G	XP_011538342.1:p.Pro1588Arg
XM_011540041.1:c.4709C>G	XP_011538343.1:p.Pro1570Arg
XM_011540042.1:c.4769C>G	XP_011538344.1:p.Pro1590Arg
XM_011540043.1:c.4769C>G	XP_011538345.1:p.Pro1590Arg
XM_011540044.1:c.4634C>G	XP_011538346.1:p.Pro1545Arg
XM_011540045.1:c.4769C>G	XP_011538347.1:p.Pro1590Arg
XM_011540046.1:c.4229C>G	XP_011538348.1:p.Pro1410Arg
XM_011540047.1:c.3587C>G	XP_011538349.1:p.Pro1196Arg
XM_011540048.1:c.4769C>G	XP_011538350.1:p.Pro1590Arg
XM_011540049.1:c.4769C>G	XP_011538351.1:p.Pro1590Arg
XM_011540050.1:c.4769C>G	XP_011538352.1:p.Pro1590Arg
XM_011540051.1:c.4769C>G	XP_011538353.1:p.Pro1590Arg
XM_011540052.1:c.1097C>G	XP_011538354.1:p.Pro366Arg
XM_011540053.1:c.4769C>G	XP_011538355.1:p.Pro1590Arg
XR_945796.1:n.5012C>G
NM_022124.6:c.4574C>G MANE Select	NP_071407.4:p.Pro1525Arg