Canonical Allele Identifier: CA929791334
Gene: CDH23 HGNC NCBI

Linked Data

dbSNP Id: rs757448884

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71793351G>A , CM000672.2:g.71793351G>A GRCh38
NC_000010.10:g.73553108G>A , CM000672.1:g.73553108G>A GRCh37
NC_000010.9:g.73223114G>A NCBI36
NG_008835.1:g.401405G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.6423G>A MANE Select ENSP00000224721.9:p.Arg2141=
ENST00000224721.10:c.6438G>A ENSP00000224721.8:p.Arg2146=
ENST00000622827.4:c.6423G>A ENSP00000483211.1:p.Arg2141=
NM_022124.5:c.6423G>A NP_071407.4:p.Arg2141=
XM_006717940.2:c.6618G>A XP_006718003.1:p.Arg2206=
XM_006717942.2:c.6552G>A XP_006718005.1:p.Arg2184=
XM_011540039.1:c.6615G>A XP_011538341.1:p.Arg2205=
XM_011540040.1:c.6612G>A XP_011538342.1:p.Arg2204=
XM_011540041.1:c.6558G>A XP_011538343.1:p.Arg2186=
XM_011540042.1:c.6577+41G>A XP_011538344.1:n.6577+41G>A
XM_011540043.1:c.6618G>A XP_011538345.1:p.Arg2206=
XM_011540044.1:c.6483G>A XP_011538346.1:p.Arg2161=
XM_011540045.1:c.6618G>A XP_011538347.1:p.Arg2206=
XM_011540046.1:c.6078G>A XP_011538348.1:p.Arg2026=
XM_011540047.1:c.5436G>A XP_011538349.1:p.Arg1812=
XM_011540048.1:c.6618G>A XP_011538350.1:p.Arg2206=
XM_011540049.1:c.6618G>A XP_011538351.1:p.Arg2206=
XM_011540050.1:c.6618G>A XP_011538352.1:p.Arg2206=
XM_011540051.1:c.6618G>A XP_011538353.1:p.Arg2206=
XM_011540052.1:c.2946G>A XP_011538354.1:p.Arg982=
XR_945796.1:n.6861G>A
NM_022124.6:c.6423G>A MANE Select NP_071407.4:p.Arg2141=