Canonical Allele Identifier: CA377150818

Gene: CDH23

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71790359A>T , CM000672.2:g.71790359A>T	GRCh38
NC_000010.10:g.73550116A>T , CM000672.1:g.73550116A>T	GRCh37
NC_000010.9:g.73220122A>T	NCBI36
NG_008835.1:g.398413A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.5995A>T MANE Select	ENSP00000224721.9:p.Thr1999Ser
ENST00000224721.10:c.6010A>T	ENSP00000224721.8:p.Thr2004Ser
ENST00000622827.4:c.5995A>T	ENSP00000483211.1:p.Thr1999Ser
NM_022124.5:c.5995A>T	NP_071407.4:p.Thr1999Ser
XM_006717940.2:c.6190A>T	XP_006718003.1:p.Thr2064Ser
XM_006717942.2:c.6124A>T	XP_006718005.1:p.Thr2042Ser
XM_011540039.1:c.6187A>T	XP_011538341.1:p.Thr2063Ser
XM_011540040.1:c.6184A>T	XP_011538342.1:p.Thr2062Ser
XM_011540041.1:c.6130A>T	XP_011538343.1:p.Thr2044Ser
XM_011540042.1:c.6190A>T	XP_011538344.1:p.Thr2064Ser
XM_011540043.1:c.6190A>T	XP_011538345.1:p.Thr2064Ser
XM_011540044.1:c.6055A>T	XP_011538346.1:p.Thr2019Ser
XM_011540045.1:c.6190A>T	XP_011538347.1:p.Thr2064Ser
XM_011540046.1:c.5650A>T	XP_011538348.1:p.Thr1884Ser
XM_011540047.1:c.5008A>T	XP_011538349.1:p.Thr1670Ser
XM_011540048.1:c.6190A>T	XP_011538350.1:p.Thr2064Ser
XM_011540049.1:c.6190A>T	XP_011538351.1:p.Thr2064Ser
XM_011540050.1:c.6190A>T	XP_011538352.1:p.Thr2064Ser
XM_011540051.1:c.6190A>T	XP_011538353.1:p.Thr2064Ser
XM_011540052.1:c.2518A>T	XP_011538354.1:p.Thr840Ser
XR_945796.1:n.6433A>T
NM_022124.6:c.5995A>T MANE Select	NP_071407.4:p.Thr1999Ser