Canonical Allele Identifier: CA377150562

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73550080G>C (hg19) ; chr10:g.71790323G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71790323G>C , CM000672.2:g.71790323G>C	GRCh38
NC_000010.10:g.73550080G>C , CM000672.1:g.73550080G>C	GRCh37
NC_000010.9:g.73220086G>C	NCBI36
NG_008835.1:g.398377G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.5959G>C MANE Select	ENSP00000224721.9:p.Ala1987Pro
ENST00000224721.10:c.5974G>C	ENSP00000224721.8:p.Ala1992Pro
ENST00000622827.4:c.5959G>C	ENSP00000483211.1:p.Ala1987Pro
NM_022124.5:c.5959G>C	NP_071407.4:p.Ala1987Pro
XM_006717940.2:c.6154G>C	XP_006718003.1:p.Ala2052Pro
XM_006717942.2:c.6088G>C	XP_006718005.1:p.Ala2030Pro
XM_011540039.1:c.6151G>C	XP_011538341.1:p.Ala2051Pro
XM_011540040.1:c.6148G>C	XP_011538342.1:p.Ala2050Pro
XM_011540041.1:c.6094G>C	XP_011538343.1:p.Ala2032Pro
XM_011540042.1:c.6154G>C	XP_011538344.1:p.Ala2052Pro
XM_011540043.1:c.6154G>C	XP_011538345.1:p.Ala2052Pro
XM_011540044.1:c.6019G>C	XP_011538346.1:p.Ala2007Pro
XM_011540045.1:c.6154G>C	XP_011538347.1:p.Ala2052Pro
XM_011540046.1:c.5614G>C	XP_011538348.1:p.Ala1872Pro
XM_011540047.1:c.4972G>C	XP_011538349.1:p.Ala1658Pro
XM_011540048.1:c.6154G>C	XP_011538350.1:p.Ala2052Pro
XM_011540049.1:c.6154G>C	XP_011538351.1:p.Ala2052Pro
XM_011540050.1:c.6154G>C	XP_011538352.1:p.Ala2052Pro
XM_011540051.1:c.6154G>C	XP_011538353.1:p.Ala2052Pro
XM_011540052.1:c.2482G>C	XP_011538354.1:p.Ala828Pro
XR_945796.1:n.6397G>C
NM_022124.6:c.5959G>C MANE Select	NP_071407.4:p.Ala1987Pro