Canonical Allele Identifier: CA5544501
Gene: CDH23 HGNC NCBI

Linked Data

dbSNP Id: rs781267543

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71709161G>C , CM000672.2:g.71709161G>C GRCh38
NC_000010.10:g.73468918G>C , CM000672.1:g.73468918G>C GRCh37
NC_000010.9:g.73138924G>C NCBI36
NG_008835.1:g.317215G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.3170G>C MANE Select ENSP00000224721.9:p.Gly1057Ala
ENST00000398809.9:c.3170G>C ENSP00000381789.5:p.Gly1057Ala
ENST00000442677.4:c.3170G>C ENSP00000388894.3:p.Gly1057Ala
ENST00000466757.8:c.2601G>C
ENST00000224721.10:c.3185G>C ENSP00000224721.8:p.Gly1062Ala
ENST00000398809.8:c.3170G>C ENSP00000381789.5:p.Gly1057Ala
ENST00000442677.3:c.1945G>C
ENST00000466757.7:c.2601G>C
ENST00000616684.4:c.3170G>C ENSP00000482036.2:p.Gly1057Ala
ENST00000622827.4:c.3170G>C ENSP00000483211.1:p.Gly1057Ala
NM_001171930.1:c.3170G>C NP_001165401.1:p.Gly1057Ala
NM_022124.5:c.3170G>C NP_071407.4:p.Gly1057Ala
XM_006717940.2:c.3365G>C XP_006718003.1:p.Gly1122Ala
XM_006717942.2:c.3299G>C XP_006718005.1:p.Gly1100Ala
XM_011540039.1:c.3365G>C XP_011538341.1:p.Gly1122Ala
XM_011540040.1:c.3359G>C XP_011538342.1:p.Gly1120Ala
XM_011540041.1:c.3305G>C XP_011538343.1:p.Gly1102Ala
XM_011540042.1:c.3365G>C XP_011538344.1:p.Gly1122Ala
XM_011540043.1:c.3365G>C XP_011538345.1:p.Gly1122Ala
XM_011540044.1:c.3230G>C XP_011538346.1:p.Gly1077Ala
XM_011540045.1:c.3365G>C XP_011538347.1:p.Gly1122Ala
XM_011540046.1:c.2825G>C XP_011538348.1:p.Gly942Ala
XM_011540047.1:c.2183G>C XP_011538349.1:p.Gly728Ala
XM_011540048.1:c.3365G>C XP_011538350.1:p.Gly1122Ala
XM_011540049.1:c.3365G>C XP_011538351.1:p.Gly1122Ala
XM_011540050.1:c.3365G>C XP_011538352.1:p.Gly1122Ala
XM_011540051.1:c.3365G>C XP_011538353.1:p.Gly1122Ala
XM_011540053.1:c.3365G>C XP_011538355.1:p.Gly1122Ala
XR_945796.1:n.3608G>C
NM_001171930.2:c.3170G>C NP_001165401.1:p.Gly1057Ala
NM_022124.6:c.3170G>C MANE Select NP_071407.4:p.Gly1057Ala