Canonical Allele Identifier: CA377154690

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73553071A>C (hg19) ; chr10:g.71793314A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793314A>C , CM000672.2:g.71793314A>C	GRCh38
NC_000010.10:g.73553071A>C , CM000672.1:g.73553071A>C	GRCh37
NC_000010.9:g.73223077A>C	NCBI36
NG_008835.1:g.401368A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6386A>C MANE Select	ENSP00000224721.9:p.Asn2129Thr
ENST00000224721.10:c.6401A>C	ENSP00000224721.8:p.Asn2134Thr
ENST00000622827.4:c.6386A>C	ENSP00000483211.1:p.Asn2129Thr
NM_022124.5:c.6386A>C	NP_071407.4:p.Asn2129Thr
XM_006717940.2:c.6581A>C	XP_006718003.1:p.Asn2194Thr
XM_006717942.2:c.6515A>C	XP_006718005.1:p.Asn2172Thr
XM_011540039.1:c.6578A>C	XP_011538341.1:p.Asn2193Thr
XM_011540040.1:c.6575A>C	XP_011538342.1:p.Asn2192Thr
XM_011540041.1:c.6521A>C	XP_011538343.1:p.Asn2174Thr
XM_011540042.1:c.6577+4A>C	XP_011538344.1:n.6577+4A>C
XM_011540043.1:c.6581A>C	XP_011538345.1:p.Asn2194Thr
XM_011540044.1:c.6446A>C	XP_011538346.1:p.Asn2149Thr
XM_011540045.1:c.6581A>C	XP_011538347.1:p.Asn2194Thr
XM_011540046.1:c.6041A>C	XP_011538348.1:p.Asn2014Thr
XM_011540047.1:c.5399A>C	XP_011538349.1:p.Asn1800Thr
XM_011540048.1:c.6581A>C	XP_011538350.1:p.Asn2194Thr
XM_011540049.1:c.6581A>C	XP_011538351.1:p.Asn2194Thr
XM_011540050.1:c.6581A>C	XP_011538352.1:p.Asn2194Thr
XM_011540051.1:c.6581A>C	XP_011538353.1:p.Asn2194Thr
XM_011540052.1:c.2909A>C	XP_011538354.1:p.Asn970Thr
XR_945796.1:n.6824A>C
NM_022124.6:c.6386A>C MANE Select	NP_071407.4:p.Asn2129Thr