Canonical Allele Identifier: CA377154376

Gene: CDH23

Linked Data

• gnomAD v4: 10-71793262-G-T
• MyVariant Identifiers: chr10:g.73553019G>T (hg19) ; chr10:g.71793262G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793262G>T , CM000672.2:g.71793262G>T	GRCh38
NC_000010.10:g.73553019G>T , CM000672.1:g.73553019G>T	GRCh37
NC_000010.9:g.73223025G>T	NCBI36
NG_008835.1:g.401316G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6334G>T MANE Select	ENSP00000224721.9:p.Ala2112Ser
ENST00000224721.10:c.6349G>T	ENSP00000224721.8:p.Ala2117Ser
ENST00000622827.4:c.6334G>T	ENSP00000483211.1:p.Ala2112Ser
NM_022124.5:c.6334G>T	NP_071407.4:p.Ala2112Ser
XM_006717940.2:c.6529G>T	XP_006718003.1:p.Ala2177Ser
XM_006717942.2:c.6463G>T	XP_006718005.1:p.Ala2155Ser
XM_011540039.1:c.6526G>T	XP_011538341.1:p.Ala2176Ser
XM_011540040.1:c.6523G>T	XP_011538342.1:p.Ala2175Ser
XM_011540041.1:c.6469G>T	XP_011538343.1:p.Ala2157Ser
XM_011540042.1:c.6529G>T	XP_011538344.1:p.Ala2177Ser
XM_011540043.1:c.6529G>T	XP_011538345.1:p.Ala2177Ser
XM_011540044.1:c.6394G>T	XP_011538346.1:p.Ala2132Ser
XM_011540045.1:c.6529G>T	XP_011538347.1:p.Ala2177Ser
XM_011540046.1:c.5989G>T	XP_011538348.1:p.Ala1997Ser
XM_011540047.1:c.5347G>T	XP_011538349.1:p.Ala1783Ser
XM_011540048.1:c.6529G>T	XP_011538350.1:p.Ala2177Ser
XM_011540049.1:c.6529G>T	XP_011538351.1:p.Ala2177Ser
XM_011540050.1:c.6529G>T	XP_011538352.1:p.Ala2177Ser
XM_011540051.1:c.6529G>T	XP_011538353.1:p.Ala2177Ser
XM_011540052.1:c.2857G>T	XP_011538354.1:p.Ala953Ser
XR_945796.1:n.6772G>T
NM_022124.6:c.6334G>T MANE Select	NP_071407.4:p.Ala2112Ser