Canonical Allele Identifier: CA470062344

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73468859C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71709102C>A , CM000672.2:g.71709102C>A	GRCh38
NC_000010.10:g.73468859C>A , CM000672.1:g.73468859C>A	GRCh37
NC_000010.9:g.73138865C>A	NCBI36
NG_008835.1:g.317156C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.3111C>A MANE Select	ENSP00000224721.9:p.Gly1037=
ENST00000398809.9:c.3111C>A	ENSP00000381789.5:p.Gly1037=
ENST00000442677.4:c.3111C>A	ENSP00000388894.3:p.Gly1037=
ENST00000466757.8:c.2542C>A
ENST00000224721.10:c.3126C>A	ENSP00000224721.8:p.Gly1042=
ENST00000398809.8:c.3111C>A	ENSP00000381789.5:p.Gly1037=
ENST00000442677.3:c.1886C>A
ENST00000466757.7:c.2542C>A
ENST00000616684.4:c.3111C>A	ENSP00000482036.2:p.Gly1037=
ENST00000622827.4:c.3111C>A	ENSP00000483211.1:p.Gly1037=
NM_001171930.1:c.3111C>A	NP_001165401.1:p.Gly1037=
NM_022124.5:c.3111C>A	NP_071407.4:p.Gly1037=
XM_006717940.2:c.3306C>A	XP_006718003.1:p.Gly1102=
XM_006717942.2:c.3240C>A	XP_006718005.1:p.Gly1080=
XM_011540039.1:c.3306C>A	XP_011538341.1:p.Gly1102=
XM_011540040.1:c.3300C>A	XP_011538342.1:p.Gly1100=
XM_011540041.1:c.3246C>A	XP_011538343.1:p.Gly1082=
XM_011540042.1:c.3306C>A	XP_011538344.1:p.Gly1102=
XM_011540043.1:c.3306C>A	XP_011538345.1:p.Gly1102=
XM_011540044.1:c.3171C>A	XP_011538346.1:p.Gly1057=
XM_011540045.1:c.3306C>A	XP_011538347.1:p.Gly1102=
XM_011540046.1:c.2766C>A	XP_011538348.1:p.Gly922=
XM_011540047.1:c.2124C>A	XP_011538349.1:p.Gly708=
XM_011540048.1:c.3306C>A	XP_011538350.1:p.Gly1102=
XM_011540049.1:c.3306C>A	XP_011538351.1:p.Gly1102=
XM_011540050.1:c.3306C>A	XP_011538352.1:p.Gly1102=
XM_011540051.1:c.3306C>A	XP_011538353.1:p.Gly1102=
XM_011540053.1:c.3306C>A	XP_011538355.1:p.Gly1102=
XR_945796.1:n.3549C>A
NM_001171930.2:c.3111C>A	NP_001165401.1:p.Gly1037=
NM_022124.6:c.3111C>A MANE Select	NP_071407.4:p.Gly1037=