Canonical Allele Identifier: CA377143411

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73468953A>G (hg19) ; chr10:g.71709196A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71709196A>G , CM000672.2:g.71709196A>G	GRCh38
NC_000010.10:g.73468953A>G , CM000672.1:g.73468953A>G	GRCh37
NC_000010.9:g.73138959A>G	NCBI36
NG_008835.1:g.317250A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.3205A>G MANE Select	ENSP00000224721.9:p.Ile1069Val
ENST00000398809.9:c.3205A>G	ENSP00000381789.5:p.Ile1069Val
ENST00000442677.4:c.3205A>G	ENSP00000388894.3:p.Ile1069Val
ENST00000466757.8:c.2636A>G
ENST00000224721.10:c.3220A>G	ENSP00000224721.8:p.Ile1074Val
ENST00000398809.8:c.3205A>G	ENSP00000381789.5:p.Ile1069Val
ENST00000442677.3:c.1980A>G
ENST00000466757.7:c.2636A>G
ENST00000616684.4:c.3205A>G	ENSP00000482036.2:p.Ile1069Val
ENST00000622827.4:c.3205A>G	ENSP00000483211.1:p.Ile1069Val
NM_001171930.1:c.3205A>G	NP_001165401.1:p.Ile1069Val
NM_022124.5:c.3205A>G	NP_071407.4:p.Ile1069Val
XM_006717940.2:c.3400A>G	XP_006718003.1:p.Ile1134Val
XM_006717942.2:c.3334A>G	XP_006718005.1:p.Ile1112Val
XM_011540039.1:c.3400A>G	XP_011538341.1:p.Ile1134Val
XM_011540040.1:c.3394A>G	XP_011538342.1:p.Ile1132Val
XM_011540041.1:c.3340A>G	XP_011538343.1:p.Ile1114Val
XM_011540042.1:c.3400A>G	XP_011538344.1:p.Ile1134Val
XM_011540043.1:c.3400A>G	XP_011538345.1:p.Ile1134Val
XM_011540044.1:c.3265A>G	XP_011538346.1:p.Ile1089Val
XM_011540045.1:c.3400A>G	XP_011538347.1:p.Ile1134Val
XM_011540046.1:c.2860A>G	XP_011538348.1:p.Ile954Val
XM_011540047.1:c.2218A>G	XP_011538349.1:p.Ile740Val
XM_011540048.1:c.3400A>G	XP_011538350.1:p.Ile1134Val
XM_011540049.1:c.3400A>G	XP_011538351.1:p.Ile1134Val
XM_011540050.1:c.3400A>G	XP_011538352.1:p.Ile1134Val
XM_011540051.1:c.3400A>G	XP_011538353.1:p.Ile1134Val
XM_011540053.1:c.3400A>G	XP_011538355.1:p.Ile1134Val
XR_945796.1:n.3643A>G
NM_001171930.2:c.3205A>G	NP_001165401.1:p.Ile1069Val
NM_022124.6:c.3205A>G MANE Select	NP_071407.4:p.Ile1069Val