Canonical Allele Identifier: CA377155183

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73553179A>T (hg19) ; chr10:g.71793422A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793422A>T , CM000672.2:g.71793422A>T	GRCh38
NC_000010.10:g.73553179A>T , CM000672.1:g.73553179A>T	GRCh37
NC_000010.9:g.73223185A>T	NCBI36
NG_008835.1:g.401476A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6494A>T MANE Select	ENSP00000224721.9:p.Asp2165Val
ENST00000224721.10:c.6509A>T	ENSP00000224721.8:p.Asp2170Val
ENST00000622827.4:c.6494A>T	ENSP00000483211.1:p.Asp2165Val
NM_022124.5:c.6494A>T	NP_071407.4:p.Asp2165Val
XM_006717940.2:c.6689A>T	XP_006718003.1:p.Asp2230Val
XM_006717942.2:c.6623A>T	XP_006718005.1:p.Asp2208Val
XM_011540039.1:c.6686A>T	XP_011538341.1:p.Asp2229Val
XM_011540040.1:c.6683A>T	XP_011538342.1:p.Asp2228Val
XM_011540041.1:c.6629A>T	XP_011538343.1:p.Asp2210Val
XM_011540042.1:c.6599A>T	XP_011538344.1:p.Asp2200Val
XM_011540043.1:c.6689A>T	XP_011538345.1:p.Asp2230Val
XM_011540044.1:c.6554A>T	XP_011538346.1:p.Asp2185Val
XM_011540045.1:c.6689A>T	XP_011538347.1:p.Asp2230Val
XM_011540046.1:c.6149A>T	XP_011538348.1:p.Asp2050Val
XM_011540047.1:c.5507A>T	XP_011538349.1:p.Asp1836Val
XM_011540048.1:c.6689A>T	XP_011538350.1:p.Asp2230Val
XM_011540049.1:c.6689A>T	XP_011538351.1:p.Asp2230Val
XM_011540050.1:c.6689A>T	XP_011538352.1:p.Asp2230Val
XM_011540051.1:c.6689A>T	XP_011538353.1:p.Asp2230Val
XM_011540052.1:c.3017A>T	XP_011538354.1:p.Asp1006Val
XR_945796.1:n.6932A>T
NM_022124.6:c.6494A>T MANE Select	NP_071407.4:p.Asp2165Val