Canonical Allele Identifier: CA377154899
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71793340G>T , CM000672.2:g.71793340G>T GRCh38
NC_000010.10:g.73553097G>T , CM000672.1:g.73553097G>T GRCh37
NC_000010.9:g.73223103G>T NCBI36
NG_008835.1:g.401394G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.6412G>T MANE Select ENSP00000224721.9:p.Glu2138Ter
ENST00000224721.10:c.6427G>T ENSP00000224721.8:p.Glu2143Ter
ENST00000622827.4:c.6412G>T ENSP00000483211.1:p.Glu2138Ter
NM_022124.5:c.6412G>T NP_071407.4:p.Glu2138Ter
XM_006717940.2:c.6607G>T XP_006718003.1:p.Glu2203Ter
XM_006717942.2:c.6541G>T XP_006718005.1:p.Glu2181Ter
XM_011540039.1:c.6604G>T XP_011538341.1:p.Glu2202Ter
XM_011540040.1:c.6601G>T XP_011538342.1:p.Glu2201Ter
XM_011540041.1:c.6547G>T XP_011538343.1:p.Glu2183Ter
XM_011540042.1:c.6577+30G>T XP_011538344.1:n.6577+30G>T
XM_011540043.1:c.6607G>T XP_011538345.1:p.Glu2203Ter
XM_011540044.1:c.6472G>T XP_011538346.1:p.Glu2158Ter
XM_011540045.1:c.6607G>T XP_011538347.1:p.Glu2203Ter
XM_011540046.1:c.6067G>T XP_011538348.1:p.Glu2023Ter
XM_011540047.1:c.5425G>T XP_011538349.1:p.Glu1809Ter
XM_011540048.1:c.6607G>T XP_011538350.1:p.Glu2203Ter
XM_011540049.1:c.6607G>T XP_011538351.1:p.Glu2203Ter
XM_011540050.1:c.6607G>T XP_011538352.1:p.Glu2203Ter
XM_011540051.1:c.6607G>T XP_011538353.1:p.Glu2203Ter
XM_011540052.1:c.2935G>T XP_011538354.1:p.Glu979Ter
XR_945796.1:n.6850G>T
NM_022124.6:c.6412G>T MANE Select NP_071407.4:p.Glu2138Ter