Canonical Allele Identifier: CA470069204

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73500608A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740851A>T , CM000672.2:g.71740851A>T	GRCh38
NC_000010.10:g.73500608A>T , CM000672.1:g.73500608A>T	GRCh37
NC_000010.9:g.73170614A>T	NCBI36
NG_008835.1:g.348905A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.4518A>T MANE Select	ENSP00000224721.9:p.Pro1506=
ENST00000224721.10:c.4533A>T	ENSP00000224721.8:p.Pro1511=
ENST00000398792.3:n.1207A>T
ENST00000622827.4:c.4518A>T	ENSP00000483211.1:p.Pro1506=
NM_022124.5:c.4518A>T	NP_071407.4:p.Pro1506=
XM_006717940.2:c.4713A>T	XP_006718003.1:p.Pro1571=
XM_006717942.2:c.4647A>T	XP_006718005.1:p.Pro1549=
XM_011540039.1:c.4710A>T	XP_011538341.1:p.Pro1570=
XM_011540040.1:c.4707A>T	XP_011538342.1:p.Pro1569=
XM_011540041.1:c.4653A>T	XP_011538343.1:p.Pro1551=
XM_011540042.1:c.4713A>T	XP_011538344.1:p.Pro1571=
XM_011540043.1:c.4713A>T	XP_011538345.1:p.Pro1571=
XM_011540044.1:c.4578A>T	XP_011538346.1:p.Pro1526=
XM_011540045.1:c.4713A>T	XP_011538347.1:p.Pro1571=
XM_011540046.1:c.4173A>T	XP_011538348.1:p.Pro1391=
XM_011540047.1:c.3531A>T	XP_011538349.1:p.Pro1177=
XM_011540048.1:c.4713A>T	XP_011538350.1:p.Pro1571=
XM_011540049.1:c.4713A>T	XP_011538351.1:p.Pro1571=
XM_011540050.1:c.4713A>T	XP_011538352.1:p.Pro1571=
XM_011540051.1:c.4713A>T	XP_011538353.1:p.Pro1571=
XM_011540052.1:c.1041A>T	XP_011538354.1:p.Pro347=
XM_011540053.1:c.4713A>T	XP_011538355.1:p.Pro1571=
XR_945796.1:n.4956A>T
NM_022124.6:c.4518A>T MANE Select	NP_071407.4:p.Pro1506=