Canonical Allele Identifier: CA377143356

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73468938G>T (hg19) ; chr10:g.71709181G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71709181G>T , CM000672.2:g.71709181G>T	GRCh38
NC_000010.10:g.73468938G>T , CM000672.1:g.73468938G>T	GRCh37
NC_000010.9:g.73138944G>T	NCBI36
NG_008835.1:g.317235G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.3190G>T MANE Select	ENSP00000224721.9:p.Ala1064Ser
ENST00000398809.9:c.3190G>T	ENSP00000381789.5:p.Ala1064Ser
ENST00000442677.4:c.3190G>T	ENSP00000388894.3:p.Ala1064Ser
ENST00000466757.8:c.2621G>T
ENST00000224721.10:c.3205G>T	ENSP00000224721.8:p.Ala1069Ser
ENST00000398809.8:c.3190G>T	ENSP00000381789.5:p.Ala1064Ser
ENST00000442677.3:c.1965G>T
ENST00000466757.7:c.2621G>T
ENST00000616684.4:c.3190G>T	ENSP00000482036.2:p.Ala1064Ser
ENST00000622827.4:c.3190G>T	ENSP00000483211.1:p.Ala1064Ser
NM_001171930.1:c.3190G>T	NP_001165401.1:p.Ala1064Ser
NM_022124.5:c.3190G>T	NP_071407.4:p.Ala1064Ser
XM_006717940.2:c.3385G>T	XP_006718003.1:p.Ala1129Ser
XM_006717942.2:c.3319G>T	XP_006718005.1:p.Ala1107Ser
XM_011540039.1:c.3385G>T	XP_011538341.1:p.Ala1129Ser
XM_011540040.1:c.3379G>T	XP_011538342.1:p.Ala1127Ser
XM_011540041.1:c.3325G>T	XP_011538343.1:p.Ala1109Ser
XM_011540042.1:c.3385G>T	XP_011538344.1:p.Ala1129Ser
XM_011540043.1:c.3385G>T	XP_011538345.1:p.Ala1129Ser
XM_011540044.1:c.3250G>T	XP_011538346.1:p.Ala1084Ser
XM_011540045.1:c.3385G>T	XP_011538347.1:p.Ala1129Ser
XM_011540046.1:c.2845G>T	XP_011538348.1:p.Ala949Ser
XM_011540047.1:c.2203G>T	XP_011538349.1:p.Ala735Ser
XM_011540048.1:c.3385G>T	XP_011538350.1:p.Ala1129Ser
XM_011540049.1:c.3385G>T	XP_011538351.1:p.Ala1129Ser
XM_011540050.1:c.3385G>T	XP_011538352.1:p.Ala1129Ser
XM_011540051.1:c.3385G>T	XP_011538353.1:p.Ala1129Ser
XM_011540053.1:c.3385G>T	XP_011538355.1:p.Ala1129Ser
XR_945796.1:n.3628G>T
NM_001171930.2:c.3190G>T	NP_001165401.1:p.Ala1064Ser
NM_022124.6:c.3190G>T MANE Select	NP_071407.4:p.Ala1064Ser