Canonical Allele Identifier: CA377143098

Gene: CDH23

Linked Data

• gnomAD v4: 10-71709124-G-C
• MyVariant Identifiers: chr10:g.73468881G>C (hg19) ; chr10:g.71709124G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71709124G>C , CM000672.2:g.71709124G>C	GRCh38
NC_000010.10:g.73468881G>C , CM000672.1:g.73468881G>C	GRCh37
NC_000010.9:g.73138887G>C	NCBI36
NG_008835.1:g.317178G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.3133G>C MANE Select	ENSP00000224721.9:p.Val1045Leu
ENST00000398809.9:c.3133G>C	ENSP00000381789.5:p.Val1045Leu
ENST00000442677.4:c.3133G>C	ENSP00000388894.3:p.Val1045Leu
ENST00000466757.8:c.2564G>C
ENST00000224721.10:c.3148G>C	ENSP00000224721.8:p.Val1050Leu
ENST00000398809.8:c.3133G>C	ENSP00000381789.5:p.Val1045Leu
ENST00000442677.3:c.1908G>C
ENST00000466757.7:c.2564G>C
ENST00000616684.4:c.3133G>C	ENSP00000482036.2:p.Val1045Leu
ENST00000622827.4:c.3133G>C	ENSP00000483211.1:p.Val1045Leu
NM_001171930.1:c.3133G>C	NP_001165401.1:p.Val1045Leu
NM_022124.5:c.3133G>C	NP_071407.4:p.Val1045Leu
XM_006717940.2:c.3328G>C	XP_006718003.1:p.Val1110Leu
XM_006717942.2:c.3262G>C	XP_006718005.1:p.Val1088Leu
XM_011540039.1:c.3328G>C	XP_011538341.1:p.Val1110Leu
XM_011540040.1:c.3322G>C	XP_011538342.1:p.Val1108Leu
XM_011540041.1:c.3268G>C	XP_011538343.1:p.Val1090Leu
XM_011540042.1:c.3328G>C	XP_011538344.1:p.Val1110Leu
XM_011540043.1:c.3328G>C	XP_011538345.1:p.Val1110Leu
XM_011540044.1:c.3193G>C	XP_011538346.1:p.Val1065Leu
XM_011540045.1:c.3328G>C	XP_011538347.1:p.Val1110Leu
XM_011540046.1:c.2788G>C	XP_011538348.1:p.Val930Leu
XM_011540047.1:c.2146G>C	XP_011538349.1:p.Val716Leu
XM_011540048.1:c.3328G>C	XP_011538350.1:p.Val1110Leu
XM_011540049.1:c.3328G>C	XP_011538351.1:p.Val1110Leu
XM_011540050.1:c.3328G>C	XP_011538352.1:p.Val1110Leu
XM_011540051.1:c.3328G>C	XP_011538353.1:p.Val1110Leu
XM_011540053.1:c.3328G>C	XP_011538355.1:p.Val1110Leu
XR_945796.1:n.3571G>C
NM_001171930.2:c.3133G>C	NP_001165401.1:p.Val1045Leu
NM_022124.6:c.3133G>C MANE Select	NP_071407.4:p.Val1045Leu