Canonical Allele Identifier: CA377154277
Gene: CDH23 HGNC NCBI

Linked Data

dbSNP Id: rs2132953364

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71793246C>G , CM000672.2:g.71793246C>G GRCh38
NC_000010.10:g.73553003C>G , CM000672.1:g.73553003C>G GRCh37
NC_000010.9:g.73223009C>G NCBI36
NG_008835.1:g.401300C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.6318C>G MANE Select ENSP00000224721.9:p.Tyr2106Ter
ENST00000224721.10:c.6333C>G ENSP00000224721.8:p.Tyr2111Ter
ENST00000622827.4:c.6318C>G ENSP00000483211.1:p.Tyr2106Ter
NM_022124.5:c.6318C>G NP_071407.4:p.Tyr2106Ter
XM_006717940.2:c.6513C>G XP_006718003.1:p.Tyr2171Ter
XM_006717942.2:c.6447C>G XP_006718005.1:p.Tyr2149Ter
XM_011540039.1:c.6510C>G XP_011538341.1:p.Tyr2170Ter
XM_011540040.1:c.6507C>G XP_011538342.1:p.Tyr2169Ter
XM_011540041.1:c.6453C>G XP_011538343.1:p.Tyr2151Ter
XM_011540042.1:c.6513C>G XP_011538344.1:p.Tyr2171Ter
XM_011540043.1:c.6513C>G XP_011538345.1:p.Tyr2171Ter
XM_011540044.1:c.6378C>G XP_011538346.1:p.Tyr2126Ter
XM_011540045.1:c.6513C>G XP_011538347.1:p.Tyr2171Ter
XM_011540046.1:c.5973C>G XP_011538348.1:p.Tyr1991Ter
XM_011540047.1:c.5331C>G XP_011538349.1:p.Tyr1777Ter
XM_011540048.1:c.6513C>G XP_011538350.1:p.Tyr2171Ter
XM_011540049.1:c.6513C>G XP_011538351.1:p.Tyr2171Ter
XM_011540050.1:c.6513C>G XP_011538352.1:p.Tyr2171Ter
XM_011540051.1:c.6513C>G XP_011538353.1:p.Tyr2171Ter
XM_011540052.1:c.2841C>G XP_011538354.1:p.Tyr947Ter
XR_945796.1:n.6756C>G
NM_022124.6:c.6318C>G MANE Select NP_071407.4:p.Tyr2106Ter