Canonical Allele Identifier: CA377150567

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73550081C>A (hg19) ; chr10:g.71790324C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71790324C>A , CM000672.2:g.71790324C>A	GRCh38
NC_000010.10:g.73550081C>A , CM000672.1:g.73550081C>A	GRCh37
NC_000010.9:g.73220087C>A	NCBI36
NG_008835.1:g.398378C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.5960C>A MANE Select	ENSP00000224721.9:p.Ala1987Asp
ENST00000224721.10:c.5975C>A	ENSP00000224721.8:p.Ala1992Asp
ENST00000622827.4:c.5960C>A	ENSP00000483211.1:p.Ala1987Asp
NM_022124.5:c.5960C>A	NP_071407.4:p.Ala1987Asp
XM_006717940.2:c.6155C>A	XP_006718003.1:p.Ala2052Asp
XM_006717942.2:c.6089C>A	XP_006718005.1:p.Ala2030Asp
XM_011540039.1:c.6152C>A	XP_011538341.1:p.Ala2051Asp
XM_011540040.1:c.6149C>A	XP_011538342.1:p.Ala2050Asp
XM_011540041.1:c.6095C>A	XP_011538343.1:p.Ala2032Asp
XM_011540042.1:c.6155C>A	XP_011538344.1:p.Ala2052Asp
XM_011540043.1:c.6155C>A	XP_011538345.1:p.Ala2052Asp
XM_011540044.1:c.6020C>A	XP_011538346.1:p.Ala2007Asp
XM_011540045.1:c.6155C>A	XP_011538347.1:p.Ala2052Asp
XM_011540046.1:c.5615C>A	XP_011538348.1:p.Ala1872Asp
XM_011540047.1:c.4973C>A	XP_011538349.1:p.Ala1658Asp
XM_011540048.1:c.6155C>A	XP_011538350.1:p.Ala2052Asp
XM_011540049.1:c.6155C>A	XP_011538351.1:p.Ala2052Asp
XM_011540050.1:c.6155C>A	XP_011538352.1:p.Ala2052Asp
XM_011540051.1:c.6155C>A	XP_011538353.1:p.Ala2052Asp
XM_011540052.1:c.2483C>A	XP_011538354.1:p.Ala828Asp
XR_945796.1:n.6398C>A
NM_022124.6:c.5960C>A MANE Select	NP_071407.4:p.Ala1987Asp