Canonical Allele Identifier: CA377155201
Gene: CDH23 HGNC NCBI

Linked Data

dbSNP Id: rs1433013026

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71793430A>C , CM000672.2:g.71793430A>C GRCh38
NC_000010.10:g.73553187A>C , CM000672.1:g.73553187A>C GRCh37
NC_000010.9:g.73223193A>C NCBI36
NG_008835.1:g.401484A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.6502A>C MANE Select ENSP00000224721.9:p.Asn2168His
ENST00000224721.10:c.6517A>C ENSP00000224721.8:p.Asn2173His
ENST00000622827.4:c.6502A>C ENSP00000483211.1:p.Asn2168His
NM_022124.5:c.6502A>C NP_071407.4:p.Asn2168His
XM_006717940.2:c.6697A>C XP_006718003.1:p.Asn2233His
XM_006717942.2:c.6631A>C XP_006718005.1:p.Asn2211His
XM_011540039.1:c.6694A>C XP_011538341.1:p.Asn2232His
XM_011540040.1:c.6691A>C XP_011538342.1:p.Asn2231His
XM_011540041.1:c.6637A>C XP_011538343.1:p.Asn2213His
XM_011540042.1:c.6607A>C XP_011538344.1:p.Asn2203His
XM_011540043.1:c.6697A>C XP_011538345.1:p.Asn2233His
XM_011540044.1:c.6562A>C XP_011538346.1:p.Asn2188His
XM_011540045.1:c.6697A>C XP_011538347.1:p.Asn2233His
XM_011540046.1:c.6157A>C XP_011538348.1:p.Asn2053His
XM_011540047.1:c.5515A>C XP_011538349.1:p.Asn1839His
XM_011540048.1:c.6697A>C XP_011538350.1:p.Asn2233His
XM_011540049.1:c.6697A>C XP_011538351.1:p.Asn2233His
XM_011540050.1:c.6697A>C XP_011538352.1:p.Asn2233His
XM_011540051.1:c.6697A>C XP_011538353.1:p.Asn2233His
XM_011540052.1:c.3025A>C XP_011538354.1:p.Asn1009His
XR_945796.1:n.6940A>C
NM_022124.6:c.6502A>C MANE Select NP_071407.4:p.Asn2168His