Canonical Allele Identifier: CA470062420

Gene: CDH23

Linked Data

• ClinVar Variation Id: 1629025
• ClinVar RCV Id: RCV002116435
• dbSNP Id: rs2132751471
• MyVariant Identifiers: chr10:g.73468946C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71709189C>T , CM000672.2:g.71709189C>T	GRCh38
NC_000010.10:g.73468946C>T , CM000672.1:g.73468946C>T	GRCh37
NC_000010.9:g.73138952C>T	NCBI36
NG_008835.1:g.317243C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.3198C>T MANE Select	ENSP00000224721.9:p.Tyr1066=
ENST00000398809.9:c.3198C>T	ENSP00000381789.5:p.Tyr1066=
ENST00000442677.4:c.3198C>T	ENSP00000388894.3:p.Tyr1066=
ENST00000466757.8:c.2629C>T
ENST00000224721.10:c.3213C>T	ENSP00000224721.8:p.Tyr1071=
ENST00000398809.8:c.3198C>T	ENSP00000381789.5:p.Tyr1066=
ENST00000442677.3:c.1973C>T
ENST00000466757.7:c.2629C>T
ENST00000616684.4:c.3198C>T	ENSP00000482036.2:p.Tyr1066=
ENST00000622827.4:c.3198C>T	ENSP00000483211.1:p.Tyr1066=
NM_001171930.1:c.3198C>T	NP_001165401.1:p.Tyr1066=
NM_022124.5:c.3198C>T	NP_071407.4:p.Tyr1066=
XM_006717940.2:c.3393C>T	XP_006718003.1:p.Tyr1131=
XM_006717942.2:c.3327C>T	XP_006718005.1:p.Tyr1109=
XM_011540039.1:c.3393C>T	XP_011538341.1:p.Tyr1131=
XM_011540040.1:c.3387C>T	XP_011538342.1:p.Tyr1129=
XM_011540041.1:c.3333C>T	XP_011538343.1:p.Tyr1111=
XM_011540042.1:c.3393C>T	XP_011538344.1:p.Tyr1131=
XM_011540043.1:c.3393C>T	XP_011538345.1:p.Tyr1131=
XM_011540044.1:c.3258C>T	XP_011538346.1:p.Tyr1086=
XM_011540045.1:c.3393C>T	XP_011538347.1:p.Tyr1131=
XM_011540046.1:c.2853C>T	XP_011538348.1:p.Tyr951=
XM_011540047.1:c.2211C>T	XP_011538349.1:p.Tyr737=
XM_011540048.1:c.3393C>T	XP_011538350.1:p.Tyr1131=
XM_011540049.1:c.3393C>T	XP_011538351.1:p.Tyr1131=
XM_011540050.1:c.3393C>T	XP_011538352.1:p.Tyr1131=
XM_011540051.1:c.3393C>T	XP_011538353.1:p.Tyr1131=
XM_011540053.1:c.3393C>T	XP_011538355.1:p.Tyr1131=
XR_945796.1:n.3636C>T
NM_001171930.2:c.3198C>T	NP_001165401.1:p.Tyr1066=
NM_022124.6:c.3198C>T MANE Select	NP_071407.4:p.Tyr1066=