Canonical Allele Identifier: CA377154959

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73553108G>T (hg19) ; chr10:g.71793351G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793351G>T , CM000672.2:g.71793351G>T	GRCh38
NC_000010.10:g.73553108G>T , CM000672.1:g.73553108G>T	GRCh37
NC_000010.9:g.73223114G>T	NCBI36
NG_008835.1:g.401405G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000224721.12:c.6423G>T MANE Select	ENSP00000224721.9:p.Arg2141Ser
ENST00000224721.10:c.6438G>T	ENSP00000224721.8:p.Arg2146Ser
ENST00000622827.4:c.6423G>T	ENSP00000483211.1:p.Arg2141Ser
NM_022124.5:c.6423G>T	NP_071407.4:p.Arg2141Ser
XM_006717940.2:c.6618G>T	XP_006718003.1:p.Arg2206Ser
XM_006717942.2:c.6552G>T	XP_006718005.1:p.Arg2184Ser
XM_011540039.1:c.6615G>T	XP_011538341.1:p.Arg2205Ser
XM_011540040.1:c.6612G>T	XP_011538342.1:p.Arg2204Ser
XM_011540041.1:c.6558G>T	XP_011538343.1:p.Arg2186Ser
XM_011540042.1:c.6577+41G>T	XP_011538344.1:n.6577+41G>T
XM_011540043.1:c.6618G>T	XP_011538345.1:p.Arg2206Ser
XM_011540044.1:c.6483G>T	XP_011538346.1:p.Arg2161Ser
XM_011540045.1:c.6618G>T	XP_011538347.1:p.Arg2206Ser
XM_011540046.1:c.6078G>T	XP_011538348.1:p.Arg2026Ser
XM_011540047.1:c.5436G>T	XP_011538349.1:p.Arg1812Ser
XM_011540048.1:c.6618G>T	XP_011538350.1:p.Arg2206Ser
XM_011540049.1:c.6618G>T	XP_011538351.1:p.Arg2206Ser
XM_011540050.1:c.6618G>T	XP_011538352.1:p.Arg2206Ser
XM_011540051.1:c.6618G>T	XP_011538353.1:p.Arg2206Ser
XM_011540052.1:c.2946G>T	XP_011538354.1:p.Arg982Ser
XR_945796.1:n.6861G>T
NM_022124.6:c.6423G>T MANE Select	NP_071407.4:p.Arg2141Ser