Canonical Allele Identifier: CA377146252

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73544657G>T (hg19) ; chr10:g.71784900G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71784900G>T , CM000672.2:g.71784900G>T	GRCh38
NC_000010.10:g.73544657G>T , CM000672.1:g.73544657G>T	GRCh37
NC_000010.9:g.73214663G>T	NCBI36
NG_008835.1:g.392954G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5512G>T MANE Select	ENSP00000224721.9:p.Gly1838Trp
ENST00000224721.10:c.5527G>T	ENSP00000224721.8:p.Gly1843Trp
ENST00000622827.4:c.5512G>T	ENSP00000483211.1:p.Gly1838Trp
NM_022124.5:c.5512G>T	NP_071407.4:p.Gly1838Trp
XM_006717940.2:c.5707G>T	XP_006718003.1:p.Gly1903Trp
XM_006717942.2:c.5641G>T	XP_006718005.1:p.Gly1881Trp
XM_011540039.1:c.5704G>T	XP_011538341.1:p.Gly1902Trp
XM_011540040.1:c.5701G>T	XP_011538342.1:p.Gly1901Trp
XM_011540041.1:c.5647G>T	XP_011538343.1:p.Gly1883Trp
XM_011540042.1:c.5707G>T	XP_011538344.1:p.Gly1903Trp
XM_011540043.1:c.5707G>T	XP_011538345.1:p.Gly1903Trp
XM_011540044.1:c.5572G>T	XP_011538346.1:p.Gly1858Trp
XM_011540045.1:c.5707G>T	XP_011538347.1:p.Gly1903Trp
XM_011540046.1:c.5167G>T	XP_011538348.1:p.Gly1723Trp
XM_011540047.1:c.4525G>T	XP_011538349.1:p.Gly1509Trp
XM_011540048.1:c.5707G>T	XP_011538350.1:p.Gly1903Trp
XM_011540049.1:c.5707G>T	XP_011538351.1:p.Gly1903Trp
XM_011540050.1:c.5707G>T	XP_011538352.1:p.Gly1903Trp
XM_011540051.1:c.5707G>T	XP_011538353.1:p.Gly1903Trp
XM_011540052.1:c.2035G>T	XP_011538354.1:p.Gly679Trp
XM_011540053.1:c.5707G>T	XP_011538355.1:p.Gly1903Trp
XR_945796.1:n.5950G>T
NM_022124.6:c.5512G>T MANE Select	NP_071407.4:p.Gly1838Trp