Canonical Allele Identifier: CA470061386

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73550070G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71790313G>T , CM000672.2:g.71790313G>T	GRCh38
NC_000010.10:g.73550070G>T , CM000672.1:g.73550070G>T	GRCh37
NC_000010.9:g.73220076G>T	NCBI36
NG_008835.1:g.398367G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.5949G>T MANE Select	ENSP00000224721.9:p.Gly1983=
ENST00000224721.10:c.5964G>T	ENSP00000224721.8:p.Gly1988=
ENST00000622827.4:c.5949G>T	ENSP00000483211.1:p.Gly1983=
NM_022124.5:c.5949G>T	NP_071407.4:p.Gly1983=
XM_006717940.2:c.6144G>T	XP_006718003.1:p.Gly2048=
XM_006717942.2:c.6078G>T	XP_006718005.1:p.Gly2026=
XM_011540039.1:c.6141G>T	XP_011538341.1:p.Gly2047=
XM_011540040.1:c.6138G>T	XP_011538342.1:p.Gly2046=
XM_011540041.1:c.6084G>T	XP_011538343.1:p.Gly2028=
XM_011540042.1:c.6144G>T	XP_011538344.1:p.Gly2048=
XM_011540043.1:c.6144G>T	XP_011538345.1:p.Gly2048=
XM_011540044.1:c.6009G>T	XP_011538346.1:p.Gly2003=
XM_011540045.1:c.6144G>T	XP_011538347.1:p.Gly2048=
XM_011540046.1:c.5604G>T	XP_011538348.1:p.Gly1868=
XM_011540047.1:c.4962G>T	XP_011538349.1:p.Gly1654=
XM_011540048.1:c.6144G>T	XP_011538350.1:p.Gly2048=
XM_011540049.1:c.6144G>T	XP_011538351.1:p.Gly2048=
XM_011540050.1:c.6144G>T	XP_011538352.1:p.Gly2048=
XM_011540051.1:c.6144G>T	XP_011538353.1:p.Gly2048=
XM_011540052.1:c.2472G>T	XP_011538354.1:p.Gly824=
XR_945796.1:n.6387G>T
NM_022124.6:c.5949G>T MANE Select	NP_071407.4:p.Gly1983=