Canonical Allele Identifier: CA377146784
Gene: CDH23 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71785008C>G , CM000672.2:g.71785008C>G GRCh38
NC_000010.10:g.73544765C>G , CM000672.1:g.73544765C>G GRCh37
NC_000010.9:g.73214771C>G NCBI36
NG_008835.1:g.393062C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.5620C>G MANE Select ENSP00000224721.9:p.Leu1874Val
ENST00000224721.10:c.5635C>G ENSP00000224721.8:p.Leu1879Val
ENST00000622827.4:c.5620C>G ENSP00000483211.1:p.Leu1874Val
NM_022124.5:c.5620C>G NP_071407.4:p.Leu1874Val
XM_006717940.2:c.5815C>G XP_006718003.1:p.Leu1939Val
XM_006717942.2:c.5749C>G XP_006718005.1:p.Leu1917Val
XM_011540039.1:c.5812C>G XP_011538341.1:p.Leu1938Val
XM_011540040.1:c.5809C>G XP_011538342.1:p.Leu1937Val
XM_011540041.1:c.5755C>G XP_011538343.1:p.Leu1919Val
XM_011540042.1:c.5815C>G XP_011538344.1:p.Leu1939Val
XM_011540043.1:c.5815C>G XP_011538345.1:p.Leu1939Val
XM_011540044.1:c.5680C>G XP_011538346.1:p.Leu1894Val
XM_011540045.1:c.5815C>G XP_011538347.1:p.Leu1939Val
XM_011540046.1:c.5275C>G XP_011538348.1:p.Leu1759Val
XM_011540047.1:c.4633C>G XP_011538349.1:p.Leu1545Val
XM_011540048.1:c.5815C>G XP_011538350.1:p.Leu1939Val
XM_011540049.1:c.5815C>G XP_011538351.1:p.Leu1939Val
XM_011540050.1:c.5815C>G XP_011538352.1:p.Leu1939Val
XM_011540051.1:c.5815C>G XP_011538353.1:p.Leu1939Val
XM_011540052.1:c.2143C>G XP_011538354.1:p.Leu715Val
XM_011540053.1:c.5815C>G XP_011538355.1:p.Leu1939Val
XR_945796.1:n.6058C>G
NM_022124.6:c.5620C>G MANE Select NP_071407.4:p.Leu1874Val