Canonical Allele Identifier: CA377154300

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73553009A>G (hg19) ; chr10:g.71793252A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793252A>G , CM000672.2:g.71793252A>G	GRCh38
NC_000010.10:g.73553009A>G , CM000672.1:g.73553009A>G	GRCh37
NC_000010.9:g.73223015A>G	NCBI36
NG_008835.1:g.401306A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6324A>G MANE Select	ENSP00000224721.9:p.Ile2108Met
ENST00000224721.10:c.6339A>G	ENSP00000224721.8:p.Ile2113Met
ENST00000622827.4:c.6324A>G	ENSP00000483211.1:p.Ile2108Met
NM_022124.5:c.6324A>G	NP_071407.4:p.Ile2108Met
XM_006717940.2:c.6519A>G	XP_006718003.1:p.Ile2173Met
XM_006717942.2:c.6453A>G	XP_006718005.1:p.Ile2151Met
XM_011540039.1:c.6516A>G	XP_011538341.1:p.Ile2172Met
XM_011540040.1:c.6513A>G	XP_011538342.1:p.Ile2171Met
XM_011540041.1:c.6459A>G	XP_011538343.1:p.Ile2153Met
XM_011540042.1:c.6519A>G	XP_011538344.1:p.Ile2173Met
XM_011540043.1:c.6519A>G	XP_011538345.1:p.Ile2173Met
XM_011540044.1:c.6384A>G	XP_011538346.1:p.Ile2128Met
XM_011540045.1:c.6519A>G	XP_011538347.1:p.Ile2173Met
XM_011540046.1:c.5979A>G	XP_011538348.1:p.Ile1993Met
XM_011540047.1:c.5337A>G	XP_011538349.1:p.Ile1779Met
XM_011540048.1:c.6519A>G	XP_011538350.1:p.Ile2173Met
XM_011540049.1:c.6519A>G	XP_011538351.1:p.Ile2173Met
XM_011540050.1:c.6519A>G	XP_011538352.1:p.Ile2173Met
XM_011540051.1:c.6519A>G	XP_011538353.1:p.Ile2173Met
XM_011540052.1:c.2847A>G	XP_011538354.1:p.Ile949Met
XR_945796.1:n.6762A>G
NM_022124.6:c.6324A>G MANE Select	NP_071407.4:p.Ile2108Met