Canonical Allele Identifier: CA470060732

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73544725C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71784968C>T , CM000672.2:g.71784968C>T	GRCh38
NC_000010.10:g.73544725C>T , CM000672.1:g.73544725C>T	GRCh37
NC_000010.9:g.73214731C>T	NCBI36
NG_008835.1:g.393022C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5580C>T MANE Select	ENSP00000224721.9:p.Ile1860=
ENST00000224721.10:c.5595C>T	ENSP00000224721.8:p.Ile1865=
ENST00000622827.4:c.5580C>T	ENSP00000483211.1:p.Ile1860=
NM_022124.5:c.5580C>T	NP_071407.4:p.Ile1860=
XM_006717940.2:c.5775C>T	XP_006718003.1:p.Ile1925=
XM_006717942.2:c.5709C>T	XP_006718005.1:p.Ile1903=
XM_011540039.1:c.5772C>T	XP_011538341.1:p.Ile1924=
XM_011540040.1:c.5769C>T	XP_011538342.1:p.Ile1923=
XM_011540041.1:c.5715C>T	XP_011538343.1:p.Ile1905=
XM_011540042.1:c.5775C>T	XP_011538344.1:p.Ile1925=
XM_011540043.1:c.5775C>T	XP_011538345.1:p.Ile1925=
XM_011540044.1:c.5640C>T	XP_011538346.1:p.Ile1880=
XM_011540045.1:c.5775C>T	XP_011538347.1:p.Ile1925=
XM_011540046.1:c.5235C>T	XP_011538348.1:p.Ile1745=
XM_011540047.1:c.4593C>T	XP_011538349.1:p.Ile1531=
XM_011540048.1:c.5775C>T	XP_011538350.1:p.Ile1925=
XM_011540049.1:c.5775C>T	XP_011538351.1:p.Ile1925=
XM_011540050.1:c.5775C>T	XP_011538352.1:p.Ile1925=
XM_011540051.1:c.5775C>T	XP_011538353.1:p.Ile1925=
XM_011540052.1:c.2103C>T	XP_011538354.1:p.Ile701=
XM_011540053.1:c.5775C>T	XP_011538355.1:p.Ile1925=
XR_945796.1:n.6018C>T
NM_022124.6:c.5580C>T MANE Select	NP_071407.4:p.Ile1860=