Canonical Allele Identifier: CA1918874472
Gene: CDH23 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.6502A= MANE Select ENSP00000224721.9:p.Asn2168=
ENST00000224721.10:c.6517A= ENSP00000224721.8:p.Asn2173=
ENST00000622827.4:c.6502A= ENSP00000483211.1:p.Asn2168=
NM_022124.5:c.6502A= NP_071407.4:p.Asn2168=
XM_006717940.2:c.6697A= XP_006718003.1:p.Asn2233=
XM_006717942.2:c.6631A= XP_006718005.1:p.Asn2211=
XM_011540039.1:c.6694A= XP_011538341.1:p.Asn2232=
XM_011540040.1:c.6691A= XP_011538342.1:p.Asn2231=
XM_011540041.1:c.6637A= XP_011538343.1:p.Asn2213=
XM_011540042.1:c.6607A= XP_011538344.1:p.Asn2203=
XM_011540043.1:c.6697A= XP_011538345.1:p.Asn2233=
XM_011540044.1:c.6562A= XP_011538346.1:p.Asn2188=
XM_011540045.1:c.6697A= XP_011538347.1:p.Asn2233=
XM_011540046.1:c.6157A= XP_011538348.1:p.Asn2053=
XM_011540047.1:c.5515A= XP_011538349.1:p.Asn1839=
XM_011540048.1:c.6697A= XP_011538350.1:p.Asn2233=
XM_011540049.1:c.6697A= XP_011538351.1:p.Asn2233=
XM_011540050.1:c.6697A= XP_011538352.1:p.Asn2233=
XM_011540051.1:c.6697A= XP_011538353.1:p.Asn2233=
XM_011540052.1:c.3025A= XP_011538354.1:p.Asn1009=
XR_945796.1:n.6940A=
NM_022124.6:c.6502A= MANE Select NP_071407.4:p.Asn2168=