Canonical Allele Identifier: CA377147110
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71785069A>T , CM000672.2:g.71785069A>T GRCh38
NC_000010.10:g.73544826A>T , CM000672.1:g.73544826A>T GRCh37
NC_000010.9:g.73214832A>T NCBI36
NG_008835.1:g.393123A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.5681A>T MANE Select ENSP00000224721.9:p.Asn1894Ile
ENST00000224721.10:c.5696A>T ENSP00000224721.8:p.Asn1899Ile
ENST00000622827.4:c.5681A>T ENSP00000483211.1:p.Asn1894Ile
NM_022124.5:c.5681A>T NP_071407.4:p.Asn1894Ile
XM_006717940.2:c.5876A>T XP_006718003.1:p.Asn1959Ile
XM_006717942.2:c.5810A>T XP_006718005.1:p.Asn1937Ile
XM_011540039.1:c.5873A>T XP_011538341.1:p.Asn1958Ile
XM_011540040.1:c.5870A>T XP_011538342.1:p.Asn1957Ile
XM_011540041.1:c.5816A>T XP_011538343.1:p.Asn1939Ile
XM_011540042.1:c.5876A>T XP_011538344.1:p.Asn1959Ile
XM_011540043.1:c.5876A>T XP_011538345.1:p.Asn1959Ile
XM_011540044.1:c.5741A>T XP_011538346.1:p.Asn1914Ile
XM_011540045.1:c.5876A>T XP_011538347.1:p.Asn1959Ile
XM_011540046.1:c.5336A>T XP_011538348.1:p.Asn1779Ile
XM_011540047.1:c.4694A>T XP_011538349.1:p.Asn1565Ile
XM_011540048.1:c.5876A>T XP_011538350.1:p.Asn1959Ile
XM_011540049.1:c.5876A>T XP_011538351.1:p.Asn1959Ile
XM_011540050.1:c.5876A>T XP_011538352.1:p.Asn1959Ile
XM_011540051.1:c.5876A>T XP_011538353.1:p.Asn1959Ile
XM_011540052.1:c.2204A>T XP_011538354.1:p.Asn735Ile
XM_011540053.1:c.5876A>T XP_011538355.1:p.Asn1959Ile
XR_945796.1:n.6119A>T
NM_022124.6:c.5681A>T MANE Select NP_071407.4:p.Asn1894Ile