Canonical Allele Identifier: CA377150519

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73550072C>A (hg19) ; chr10:g.71790315C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71790315C>A , CM000672.2:g.71790315C>A	GRCh38
NC_000010.10:g.73550072C>A , CM000672.1:g.73550072C>A	GRCh37
NC_000010.9:g.73220078C>A	NCBI36
NG_008835.1:g.398369C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.5951C>A MANE Select	ENSP00000224721.9:p.Pro1984His
ENST00000224721.10:c.5966C>A	ENSP00000224721.8:p.Pro1989His
ENST00000622827.4:c.5951C>A	ENSP00000483211.1:p.Pro1984His
NM_022124.5:c.5951C>A	NP_071407.4:p.Pro1984His
XM_006717940.2:c.6146C>A	XP_006718003.1:p.Pro2049His
XM_006717942.2:c.6080C>A	XP_006718005.1:p.Pro2027His
XM_011540039.1:c.6143C>A	XP_011538341.1:p.Pro2048His
XM_011540040.1:c.6140C>A	XP_011538342.1:p.Pro2047His
XM_011540041.1:c.6086C>A	XP_011538343.1:p.Pro2029His
XM_011540042.1:c.6146C>A	XP_011538344.1:p.Pro2049His
XM_011540043.1:c.6146C>A	XP_011538345.1:p.Pro2049His
XM_011540044.1:c.6011C>A	XP_011538346.1:p.Pro2004His
XM_011540045.1:c.6146C>A	XP_011538347.1:p.Pro2049His
XM_011540046.1:c.5606C>A	XP_011538348.1:p.Pro1869His
XM_011540047.1:c.4964C>A	XP_011538349.1:p.Pro1655His
XM_011540048.1:c.6146C>A	XP_011538350.1:p.Pro2049His
XM_011540049.1:c.6146C>A	XP_011538351.1:p.Pro2049His
XM_011540050.1:c.6146C>A	XP_011538352.1:p.Pro2049His
XM_011540051.1:c.6146C>A	XP_011538353.1:p.Pro2049His
XM_011540052.1:c.2474C>A	XP_011538354.1:p.Pro825His
XR_945796.1:n.6389C>A
NM_022124.6:c.5951C>A MANE Select	NP_071407.4:p.Pro1984His