Canonical Allele Identifier: CA209466039

Gene: CDH23

Linked Data

• dbSNP Id: rs16929354
• MyVariant Identifiers: chr10:g.73553060C>G (hg19) ; chr10:g.71793303C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793303C>G , CM000672.2:g.71793303C>G	GRCh38
NC_000010.10:g.73553060C>G , CM000672.1:g.73553060C>G	GRCh37
NC_000010.9:g.73223066C>G	NCBI36
NG_008835.1:g.401357C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6375C>G MANE Select	ENSP00000224721.9:p.Ile2125Met
ENST00000224721.10:c.6390C>G	ENSP00000224721.8:p.Ile2130Met
ENST00000622827.4:c.6375C>G	ENSP00000483211.1:p.Ile2125Met
NM_022124.5:c.6375C>G	NP_071407.4:p.Ile2125Met
XM_006717940.2:c.6570C>G	XP_006718003.1:p.Ile2190Met
XM_006717942.2:c.6504C>G	XP_006718005.1:p.Ile2168Met
XM_011540039.1:c.6567C>G	XP_011538341.1:p.Ile2189Met
XM_011540040.1:c.6564C>G	XP_011538342.1:p.Ile2188Met
XM_011540041.1:c.6510C>G	XP_011538343.1:p.Ile2170Met
XM_011540042.1:c.6570C>G	XP_011538344.1:p.Ile2190Met
XM_011540043.1:c.6570C>G	XP_011538345.1:p.Ile2190Met
XM_011540044.1:c.6435C>G	XP_011538346.1:p.Ile2145Met
XM_011540045.1:c.6570C>G	XP_011538347.1:p.Ile2190Met
XM_011540046.1:c.6030C>G	XP_011538348.1:p.Ile2010Met
XM_011540047.1:c.5388C>G	XP_011538349.1:p.Ile1796Met
XM_011540048.1:c.6570C>G	XP_011538350.1:p.Ile2190Met
XM_011540049.1:c.6570C>G	XP_011538351.1:p.Ile2190Met
XM_011540050.1:c.6570C>G	XP_011538352.1:p.Ile2190Met
XM_011540051.1:c.6570C>G	XP_011538353.1:p.Ile2190Met
XM_011540052.1:c.2898C>G	XP_011538354.1:p.Ile966Met
XR_945796.1:n.6813C>G
NM_022124.6:c.6375C>G MANE Select	NP_071407.4:p.Ile2125Met