Canonical Allele Identifier: CA1918874059
Gene: CDH23 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71793082_71793095delinsATGAGAAGGGGACT , CM000672.2:g.71793082_71793095delinsATGAGAAGGGGACT GRCh38
NC_000010.10:g.73552839_73552852delinsATGAGAAGGGGACT , CM000672.1:g.73552839_73552852delinsATGAGAAGGGGACT GRCh37
NC_000010.9:g.73222845_73222858delinsATGAGAAGGGGACT NCBI36
NG_008835.1:g.401136_401149delinsATGAGAAGGGGACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.6254-100_6254-87delinsATGAGAAGGGGACT MANE Select ENSP00000224721.9:n.6254-100_6254-87delinsATGAGAAGGGGACT
ENST00000224721.10:c.6269-100_6269-87delinsATGAGAAGGGGACT ENSP00000224721.8:n.6269-100_6269-87delinsATGAGAAGGGGACT
ENST00000622827.4:c.6254-100_6254-87delinsATGAGAAGGGGACT ENSP00000483211.1:n.6254-100_6254-87delinsATGAGAAGGGGACT
NM_022124.5:c.6254-100_6254-87delinsATGAGAAGGGGACT NP_071407.4:n.6254-100_6254-87delinsATGAGAAGGGGACT
XM_006717940.2:c.6449-100_6449-87delinsATGAGAAGGGGACT XP_006718003.1:n.6449-100_6449-87delinsATGAGAAGGGGACT
XM_006717942.2:c.6383-100_6383-87delinsATGAGAAGGGGACT XP_006718005.1:n.6383-100_6383-87delinsATGAGAAGGGGACT
XM_011540039.1:c.6446-100_6446-87delinsATGAGAAGGGGACT XP_011538341.1:n.6446-100_6446-87delinsATGAGAAGGGGACT
XM_011540040.1:c.6443-100_6443-87delinsATGAGAAGGGGACT XP_011538342.1:n.6443-100_6443-87delinsATGAGAAGGGGACT
XM_011540041.1:c.6389-100_6389-87delinsATGAGAAGGGGACT XP_011538343.1:n.6389-100_6389-87delinsATGAGAAGGGGACT
XM_011540042.1:c.6449-100_6449-87delinsATGAGAAGGGGACT XP_011538344.1:n.6449-100_6449-87delinsATGAGAAGGGGACT
XM_011540043.1:c.6449-100_6449-87delinsATGAGAAGGGGACT XP_011538345.1:n.6449-100_6449-87delinsATGAGAAGGGGACT
XM_011540044.1:c.6314-100_6314-87delinsATGAGAAGGGGACT XP_011538346.1:n.6314-100_6314-87delinsATGAGAAGGGGACT
XM_011540045.1:c.6449-100_6449-87delinsATGAGAAGGGGACT XP_011538347.1:n.6449-100_6449-87delinsATGAGAAGGGGACT
XM_011540046.1:c.5909-100_5909-87delinsATGAGAAGGGGACT XP_011538348.1:n.5909-100_5909-87delinsATGAGAAGGGGACT
XM_011540047.1:c.5267-100_5267-87delinsATGAGAAGGGGACT XP_011538349.1:n.5267-100_5267-87delinsATGAGAAGGGGACT
XM_011540048.1:c.6449-100_6449-87delinsATGAGAAGGGGACT XP_011538350.1:n.6449-100_6449-87delinsATGAGAAGGGGACT
XM_011540049.1:c.6449-100_6449-87delinsATGAGAAGGGGACT XP_011538351.1:n.6449-100_6449-87delinsATGAGAAGGGGACT
XM_011540050.1:c.6449-100_6449-87delinsATGAGAAGGGGACT XP_011538352.1:n.6449-100_6449-87delinsATGAGAAGGGGACT
XM_011540051.1:c.6449-100_6449-87delinsATGAGAAGGGGACT XP_011538353.1:n.6449-100_6449-87delinsATGAGAAGGGGACT
XM_011540052.1:c.2777-100_2777-87delinsATGAGAAGGGGACT XP_011538354.1:n.2777-100_2777-87delinsATGAGAAGGGGACT
XR_945796.1:n.6692-100_6692-87delinsATGAGAAGGGGACT
NM_022124.6:c.6254-100_6254-87delinsATGAGAAGGGGACT MANE Select NP_071407.4:n.6254-100_6254-87delinsATGAGAAGGGGACT