Canonical Allele Identifier: CA470069228
Gene: CDH23 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.73500644G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71740887G>C , CM000672.2:g.71740887G>C GRCh38
NC_000010.10:g.73500644G>C , CM000672.1:g.73500644G>C GRCh37
NC_000010.9:g.73170650G>C NCBI36
NG_008835.1:g.348941G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000224721.12:c.4554G>C MANE Select ENSP00000224721.9:p.Leu1518=
ENST00000224721.10:c.4569G>C ENSP00000224721.8:p.Leu1523=
ENST00000398792.3:n.1243G>C
ENST00000622827.4:c.4554G>C ENSP00000483211.1:p.Leu1518=
NM_022124.5:c.4554G>C NP_071407.4:p.Leu1518=
XM_006717940.2:c.4749G>C XP_006718003.1:p.Leu1583=
XM_006717942.2:c.4683G>C XP_006718005.1:p.Leu1561=
XM_011540039.1:c.4746G>C XP_011538341.1:p.Leu1582=
XM_011540040.1:c.4743G>C XP_011538342.1:p.Leu1581=
XM_011540041.1:c.4689G>C XP_011538343.1:p.Leu1563=
XM_011540042.1:c.4749G>C XP_011538344.1:p.Leu1583=
XM_011540043.1:c.4749G>C XP_011538345.1:p.Leu1583=
XM_011540044.1:c.4614G>C XP_011538346.1:p.Leu1538=
XM_011540045.1:c.4749G>C XP_011538347.1:p.Leu1583=
XM_011540046.1:c.4209G>C XP_011538348.1:p.Leu1403=
XM_011540047.1:c.3567G>C XP_011538349.1:p.Leu1189=
XM_011540048.1:c.4749G>C XP_011538350.1:p.Leu1583=
XM_011540049.1:c.4749G>C XP_011538351.1:p.Leu1583=
XM_011540050.1:c.4749G>C XP_011538352.1:p.Leu1583=
XM_011540051.1:c.4749G>C XP_011538353.1:p.Leu1583=
XM_011540052.1:c.1077G>C XP_011538354.1:p.Leu359=
XM_011540053.1:c.4749G>C XP_011538355.1:p.Leu1583=
XR_945796.1:n.4992G>C
NM_022124.6:c.4554G>C MANE Select NP_071407.4:p.Leu1518=