Canonical Allele Identifier: CA470282186
Gene: CDH23 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.73565946C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.71806189C>T , CM000672.2:g.71806189C>T GRCh38
NC_000010.10:g.73565946C>T , CM000672.1:g.73565946C>T GRCh37
NC_000010.9:g.73235952C>T NCBI36
NG_008835.1:g.414243C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000224721.12:c.8086C>T MANE Select ENSP00000224721.9:p.Leu2696=
ENST00000642965.1:c.2019C>T ENSP00000495222.1:n.2019C>T
ENST00000647092.1:c.1683C>T ENSP00000495176.1:n.1683C>T
ENST00000224721.10:c.8101C>T ENSP00000224721.8:p.Leu2701=
ENST00000398788.4:c.1366C>T ENSP00000381768.3:p.Leu456=
ENST00000475158.1:n.1622C>T
ENST00000619887.4:c.1366C>T ENSP00000478374.1:p.Leu456=
ENST00000622827.4:c.8086C>T ENSP00000483211.1:p.Leu2696=
NM_001171933.1:c.1366C>T NP_001165404.1:p.Leu456=
NM_001171934.1:c.1366C>T NP_001165405.1:p.Leu456=
NM_022124.5:c.8086C>T NP_071407.4:p.Leu2696=
XM_006717940.2:c.8281C>T XP_006718003.1:p.Leu2761=
XM_006717942.2:c.8215C>T XP_006718005.1:p.Leu2739=
XM_011540039.1:c.8278C>T XP_011538341.1:p.Leu2760=
XM_011540040.1:c.8275C>T XP_011538342.1:p.Leu2759=
XM_011540041.1:c.8221C>T XP_011538343.1:p.Leu2741=
XM_011540042.1:c.8191C>T XP_011538344.1:p.Leu2731=
XM_011540043.1:c.8281C>T XP_011538345.1:p.Leu2761=
XM_011540044.1:c.8146C>T XP_011538346.1:p.Leu2716=
XM_011540045.1:c.8281C>T XP_011538347.1:p.Leu2761=
XM_011540046.1:c.7741C>T XP_011538348.1:p.Leu2581=
XM_011540047.1:c.7099C>T XP_011538349.1:p.Leu2367=
XM_011540052.1:c.4609C>T XP_011538354.1:p.Leu1537=
NM_022124.6:c.8086C>T MANE Select NP_071407.4:p.Leu2696=