Canonical Allele Identifier: CA377160608

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73500657A>C (hg19) ; chr10:g.71740900A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71740900A>C , CM000672.2:g.71740900A>C	GRCh38
NC_000010.10:g.73500657A>C , CM000672.1:g.73500657A>C	GRCh37
NC_000010.9:g.73170663A>C	NCBI36
NG_008835.1:g.348954A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.4567A>C MANE Select	ENSP00000224721.9:p.Asn1523His
ENST00000224721.10:c.4582A>C	ENSP00000224721.8:p.Asn1528His
ENST00000398792.3:n.1256A>C
ENST00000622827.4:c.4567A>C	ENSP00000483211.1:p.Asn1523His
NM_022124.5:c.4567A>C	NP_071407.4:p.Asn1523His
XM_006717940.2:c.4762A>C	XP_006718003.1:p.Asn1588His
XM_006717942.2:c.4696A>C	XP_006718005.1:p.Asn1566His
XM_011540039.1:c.4759A>C	XP_011538341.1:p.Asn1587His
XM_011540040.1:c.4756A>C	XP_011538342.1:p.Asn1586His
XM_011540041.1:c.4702A>C	XP_011538343.1:p.Asn1568His
XM_011540042.1:c.4762A>C	XP_011538344.1:p.Asn1588His
XM_011540043.1:c.4762A>C	XP_011538345.1:p.Asn1588His
XM_011540044.1:c.4627A>C	XP_011538346.1:p.Asn1543His
XM_011540045.1:c.4762A>C	XP_011538347.1:p.Asn1588His
XM_011540046.1:c.4222A>C	XP_011538348.1:p.Asn1408His
XM_011540047.1:c.3580A>C	XP_011538349.1:p.Asn1194His
XM_011540048.1:c.4762A>C	XP_011538350.1:p.Asn1588His
XM_011540049.1:c.4762A>C	XP_011538351.1:p.Asn1588His
XM_011540050.1:c.4762A>C	XP_011538352.1:p.Asn1588His
XM_011540051.1:c.4762A>C	XP_011538353.1:p.Asn1588His
XM_011540052.1:c.1090A>C	XP_011538354.1:p.Asn364His
XM_011540053.1:c.4762A>C	XP_011538355.1:p.Asn1588His
XR_945796.1:n.5005A>C
NM_022124.6:c.4567A>C MANE Select	NP_071407.4:p.Asn1523His