Canonical Allele Identifier: CA2609569905

Gene: CDH23

Linked Data

• gnomAD v4: 10-71740783-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740783A>T , CM000672.2:g.71740783A>T	GRCh38
NC_000010.10:g.73500540A>T , CM000672.1:g.73500540A>T	GRCh37
NC_000010.9:g.73170546A>T	NCBI36
NG_008835.1:g.348837A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4489-39A>T MANE Select	ENSP00000224721.9:n.4489-39A>T
ENST00000224721.10:c.4504-39A>T	ENSP00000224721.8:n.4504-39A>T
ENST00000398792.3:n.1178-39A>T
ENST00000622827.4:c.4489-39A>T	ENSP00000483211.1:n.4489-39A>T
NM_022124.5:c.4489-39A>T	NP_071407.4:n.4489-39A>T
XM_006717940.2:c.4684-39A>T	XP_006718003.1:n.4684-39A>T
XM_006717942.2:c.4618-39A>T	XP_006718005.1:n.4618-39A>T
XM_011540039.1:c.4681-39A>T	XP_011538341.1:n.4681-39A>T
XM_011540040.1:c.4678-39A>T	XP_011538342.1:n.4678-39A>T
XM_011540041.1:c.4624-39A>T	XP_011538343.1:n.4624-39A>T
XM_011540042.1:c.4684-39A>T	XP_011538344.1:n.4684-39A>T
XM_011540043.1:c.4684-39A>T	XP_011538345.1:n.4684-39A>T
XM_011540044.1:c.4549-39A>T	XP_011538346.1:n.4549-39A>T
XM_011540045.1:c.4684-39A>T	XP_011538347.1:n.4684-39A>T
XM_011540046.1:c.4144-39A>T	XP_011538348.1:n.4144-39A>T
XM_011540047.1:c.3502-39A>T	XP_011538349.1:n.3502-39A>T
XM_011540048.1:c.4684-39A>T	XP_011538350.1:n.4684-39A>T
XM_011540049.1:c.4684-39A>T	XP_011538351.1:n.4684-39A>T
XM_011540050.1:c.4684-39A>T	XP_011538352.1:n.4684-39A>T
XM_011540051.1:c.4684-39A>T	XP_011538353.1:n.4684-39A>T
XM_011540052.1:c.1012-39A>T	XP_011538354.1:n.1012-39A>T
XM_011540053.1:c.4684-39A>T	XP_011538355.1:n.4684-39A>T
XR_945796.1:n.4927-39A>T
NM_022124.6:c.4489-39A>T MANE Select	NP_071407.4:n.4489-39A>T