Canonical Allele Identifier: CA377150339

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71790287G>A , CM000672.2:g.71790287G>A	GRCh38
NC_000010.10:g.73550044G>A , CM000672.1:g.73550044G>A	GRCh37
NC_000010.9:g.73220050G>A	NCBI36
NG_008835.1:g.398341G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_022124.6:c.5924-1G>A MANE Select	NP_071407.4:n.5924-1G>A
ENST00000224721.12:c.5924-1G>A MANE Select	ENSP00000224721.9:n.5924-1G>A
NM_022124.5:c.5924-1G>A	NP_071407.4:n.5924-1G>A
ENST00000224721.10:c.5939-1G>A	ENSP00000224721.8:n.5939-1G>A
ENST00000622827.4:c.5924-1G>A	ENSP00000483211.1:n.5924-1G>A
XM_006717940.2:c.6119-1G>A	XP_006718003.1:n.6119-1G>A
XM_006717942.2:c.6053-1G>A	XP_006718005.1:n.6053-1G>A
XM_011540039.1:c.6116-1G>A	XP_011538341.1:n.6116-1G>A
XM_011540040.1:c.6113-1G>A	XP_011538342.1:n.6113-1G>A
XM_011540041.1:c.6059-1G>A	XP_011538343.1:n.6059-1G>A
XM_011540042.1:c.6119-1G>A	XP_011538344.1:n.6119-1G>A
XM_011540043.1:c.6119-1G>A	XP_011538345.1:n.6119-1G>A
XM_011540044.1:c.5984-1G>A	XP_011538346.1:n.5984-1G>A
XM_011540045.1:c.6119-1G>A	XP_011538347.1:n.6119-1G>A
XM_011540046.1:c.5579-1G>A	XP_011538348.1:n.5579-1G>A
XM_011540047.1:c.4937-1G>A	XP_011538349.1:n.4937-1G>A
XM_011540048.1:c.6119-1G>A	XP_011538350.1:n.6119-1G>A
XM_011540049.1:c.6119-1G>A	XP_011538351.1:n.6119-1G>A
XM_011540050.1:c.6119-1G>A	XP_011538352.1:n.6119-1G>A
XM_011540051.1:c.6119-1G>A	XP_011538353.1:n.6119-1G>A
XM_011540052.1:c.2447-1G>A	XP_011538354.1:n.2447-1G>A
XR_945796.1:n.6362-1G>A