Canonical Allele Identifier: CA377146492

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73544685A>C (hg19) ; chr10:g.71784928A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71784928A>C , CM000672.2:g.71784928A>C	GRCh38
NC_000010.10:g.73544685A>C , CM000672.1:g.73544685A>C	GRCh37
NC_000010.9:g.73214691A>C	NCBI36
NG_008835.1:g.392982A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5540A>C MANE Select	ENSP00000224721.9:p.Asn1847Thr
ENST00000224721.10:c.5555A>C	ENSP00000224721.8:p.Asn1852Thr
ENST00000622827.4:c.5540A>C	ENSP00000483211.1:p.Asn1847Thr
NM_022124.5:c.5540A>C	NP_071407.4:p.Asn1847Thr
XM_006717940.2:c.5735A>C	XP_006718003.1:p.Asn1912Thr
XM_006717942.2:c.5669A>C	XP_006718005.1:p.Asn1890Thr
XM_011540039.1:c.5732A>C	XP_011538341.1:p.Asn1911Thr
XM_011540040.1:c.5729A>C	XP_011538342.1:p.Asn1910Thr
XM_011540041.1:c.5675A>C	XP_011538343.1:p.Asn1892Thr
XM_011540042.1:c.5735A>C	XP_011538344.1:p.Asn1912Thr
XM_011540043.1:c.5735A>C	XP_011538345.1:p.Asn1912Thr
XM_011540044.1:c.5600A>C	XP_011538346.1:p.Asn1867Thr
XM_011540045.1:c.5735A>C	XP_011538347.1:p.Asn1912Thr
XM_011540046.1:c.5195A>C	XP_011538348.1:p.Asn1732Thr
XM_011540047.1:c.4553A>C	XP_011538349.1:p.Asn1518Thr
XM_011540048.1:c.5735A>C	XP_011538350.1:p.Asn1912Thr
XM_011540049.1:c.5735A>C	XP_011538351.1:p.Asn1912Thr
XM_011540050.1:c.5735A>C	XP_011538352.1:p.Asn1912Thr
XM_011540051.1:c.5735A>C	XP_011538353.1:p.Asn1912Thr
XM_011540052.1:c.2063A>C	XP_011538354.1:p.Asn688Thr
XM_011540053.1:c.5735A>C	XP_011538355.1:p.Asn1912Thr
XR_945796.1:n.5978A>C
NM_022124.6:c.5540A>C MANE Select	NP_071407.4:p.Asn1847Thr