Canonical Allele Identifier: CA377158614

Gene: CDH23 C10orf105

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71734659G>C , CM000672.2:g.71734659G>C	GRCh38
NC_000010.10:g.73494416G>C , CM000672.1:g.73494416G>C	GRCh37
NC_000010.9:g.73164422G>C	NCBI36
NG_008835.1:g.342713G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_022124.6:c.4209+1G>C (CDH23) MANE Select	NP_071407.4:n.4209+1G>C
ENST00000224721.12:c.4209+1G>C (CDH23) MANE Select	ENSP00000224721.9:n.4209+1G>C
NM_001168390.1:c.-6+3069C>G (C10orf105)	NP_001161862.1:n.-6+3069C>G
NM_001168390.2:c.-6+3069C>G (C10orf105)	NP_001161862.1:n.-6+3069C>G
NM_022124.5:c.4209+1G>C (CDH23)	NP_071407.4:n.4209+1G>C
ENST00000224721.10:c.4224+1G>C (CDH23)	ENSP00000224721.8:n.4224+1G>C
ENST00000398786.2:c.-6+3069C>G (C10orf105)	ENSP00000381766.3:n.-6+3069C>G
ENST00000398792.3:n.898+318G>C (CDH23)
ENST00000622827.4:c.4206+318G>C (CDH23)	ENSP00000483211.1:n.4206+318G>C
XM_006717940.2:c.4404+1G>C (CDH23)	XP_006718003.1:n.4404+1G>C
XM_006717942.2:c.4338+1G>C (CDH23)	XP_006718005.1:n.4338+1G>C
XM_011540039.1:c.4401+318G>C (CDH23)	XP_011538341.1:n.4401+318G>C
XM_011540040.1:c.4398+1G>C (CDH23)	XP_011538342.1:n.4398+1G>C
XM_011540041.1:c.4344+1G>C (CDH23)	XP_011538343.1:n.4344+1G>C
XM_011540042.1:c.4404+1G>C (CDH23)	XP_011538344.1:n.4404+1G>C
XM_011540043.1:c.4404+1G>C (CDH23)	XP_011538345.1:n.4404+1G>C
XM_011540044.1:c.4269+1G>C (CDH23)	XP_011538346.1:n.4269+1G>C
XM_011540045.1:c.4404+1G>C (CDH23)	XP_011538347.1:n.4404+1G>C
XM_011540046.1:c.3864+1G>C (CDH23)	XP_011538348.1:n.3864+1G>C
XM_011540047.1:c.3222+1G>C (CDH23)	XP_011538349.1:n.3222+1G>C
XM_011540048.1:c.4404+1G>C (CDH23)	XP_011538350.1:n.4404+1G>C
XM_011540049.1:c.4404+1G>C (CDH23)	XP_011538351.1:n.4404+1G>C
XM_011540050.1:c.4404+1G>C (CDH23)	XP_011538352.1:n.4404+1G>C
XM_011540051.1:c.4404+1G>C (CDH23)	XP_011538353.1:n.4404+1G>C
XM_011540052.1:c.732+1G>C (CDH23)	XP_011538354.1:n.732+1G>C
XM_011540053.1:c.4404+1G>C (CDH23)	XP_011538355.1:n.4404+1G>C
XR_945796.1:n.4647+1G>C (CDH23)