Canonical Allele Identifier: CA377160496

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73500631A>G (hg19) ; chr10:g.71740874A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740874A>G , CM000672.2:g.71740874A>G	GRCh38
NC_000010.10:g.73500631A>G , CM000672.1:g.73500631A>G	GRCh37
NC_000010.9:g.73170637A>G	NCBI36
NG_008835.1:g.348928A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4541A>G MANE Select	ENSP00000224721.9:p.Gln1514Arg
ENST00000224721.10:c.4556A>G	ENSP00000224721.8:p.Gln1519Arg
ENST00000398792.3:n.1230A>G
ENST00000622827.4:c.4541A>G	ENSP00000483211.1:p.Gln1514Arg
NM_022124.5:c.4541A>G	NP_071407.4:p.Gln1514Arg
XM_006717940.2:c.4736A>G	XP_006718003.1:p.Gln1579Arg
XM_006717942.2:c.4670A>G	XP_006718005.1:p.Gln1557Arg
XM_011540039.1:c.4733A>G	XP_011538341.1:p.Gln1578Arg
XM_011540040.1:c.4730A>G	XP_011538342.1:p.Gln1577Arg
XM_011540041.1:c.4676A>G	XP_011538343.1:p.Gln1559Arg
XM_011540042.1:c.4736A>G	XP_011538344.1:p.Gln1579Arg
XM_011540043.1:c.4736A>G	XP_011538345.1:p.Gln1579Arg
XM_011540044.1:c.4601A>G	XP_011538346.1:p.Gln1534Arg
XM_011540045.1:c.4736A>G	XP_011538347.1:p.Gln1579Arg
XM_011540046.1:c.4196A>G	XP_011538348.1:p.Gln1399Arg
XM_011540047.1:c.3554A>G	XP_011538349.1:p.Gln1185Arg
XM_011540048.1:c.4736A>G	XP_011538350.1:p.Gln1579Arg
XM_011540049.1:c.4736A>G	XP_011538351.1:p.Gln1579Arg
XM_011540050.1:c.4736A>G	XP_011538352.1:p.Gln1579Arg
XM_011540051.1:c.4736A>G	XP_011538353.1:p.Gln1579Arg
XM_011540052.1:c.1064A>G	XP_011538354.1:p.Gln355Arg
XM_011540053.1:c.4736A>G	XP_011538355.1:p.Gln1579Arg
XR_945796.1:n.4979A>G
NM_022124.6:c.4541A>G MANE Select	NP_071407.4:p.Gln1514Arg