Canonical Allele Identifier: CA470060813

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73544857G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71785100G>T , CM000672.2:g.71785100G>T	GRCh38
NC_000010.10:g.73544857G>T , CM000672.1:g.73544857G>T	GRCh37
NC_000010.9:g.73214863G>T	NCBI36
NG_008835.1:g.393154G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5712G>T MANE Select	ENSP00000224721.9:p.Thr1904=
ENST00000224721.10:c.5727G>T	ENSP00000224721.8:p.Thr1909=
ENST00000622827.4:c.5712G>T	ENSP00000483211.1:p.Thr1904=
NM_022124.5:c.5712G>T	NP_071407.4:p.Thr1904=
XM_006717940.2:c.5907G>T	XP_006718003.1:p.Thr1969=
XM_006717942.2:c.5841G>T	XP_006718005.1:p.Thr1947=
XM_011540039.1:c.5904G>T	XP_011538341.1:p.Thr1968=
XM_011540040.1:c.5901G>T	XP_011538342.1:p.Thr1967=
XM_011540041.1:c.5847G>T	XP_011538343.1:p.Thr1949=
XM_011540042.1:c.5907G>T	XP_011538344.1:p.Thr1969=
XM_011540043.1:c.5907G>T	XP_011538345.1:p.Thr1969=
XM_011540044.1:c.5772G>T	XP_011538346.1:p.Thr1924=
XM_011540045.1:c.5907G>T	XP_011538347.1:p.Thr1969=
XM_011540046.1:c.5367G>T	XP_011538348.1:p.Thr1789=
XM_011540047.1:c.4725G>T	XP_011538349.1:p.Thr1575=
XM_011540048.1:c.5907G>T	XP_011538350.1:p.Thr1969=
XM_011540049.1:c.5907G>T	XP_011538351.1:p.Thr1969=
XM_011540050.1:c.5907G>T	XP_011538352.1:p.Thr1969=
XM_011540051.1:c.5907G>T	XP_011538353.1:p.Thr1969=
XM_011540052.1:c.2235G>T	XP_011538354.1:p.Thr745=
XM_011540053.1:c.5907G>T	XP_011538355.1:p.Thr1969=
XR_945796.1:n.6150G>T
NM_022124.6:c.5712G>T MANE Select	NP_071407.4:p.Thr1904=