Canonical Allele Identifier: CA377154466

Gene: CDH23

Linked Data

• MyVariant Identifiers: chr10:g.73553032T>C (hg19) ; chr10:g.71793275T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.71793275T>C , CM000672.2:g.71793275T>C	GRCh38
NC_000010.10:g.73553032T>C , CM000672.1:g.73553032T>C	GRCh37
NC_000010.9:g.73223038T>C	NCBI36
NG_008835.1:g.401329T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000224721.12:c.6347T>C MANE Select	ENSP00000224721.9:p.Phe2116Ser
ENST00000224721.10:c.6362T>C	ENSP00000224721.8:p.Phe2121Ser
ENST00000622827.4:c.6347T>C	ENSP00000483211.1:p.Phe2116Ser
NM_022124.5:c.6347T>C	NP_071407.4:p.Phe2116Ser
XM_006717940.2:c.6542T>C	XP_006718003.1:p.Phe2181Ser
XM_006717942.2:c.6476T>C	XP_006718005.1:p.Phe2159Ser
XM_011540039.1:c.6539T>C	XP_011538341.1:p.Phe2180Ser
XM_011540040.1:c.6536T>C	XP_011538342.1:p.Phe2179Ser
XM_011540041.1:c.6482T>C	XP_011538343.1:p.Phe2161Ser
XM_011540042.1:c.6542T>C	XP_011538344.1:p.Phe2181Ser
XM_011540043.1:c.6542T>C	XP_011538345.1:p.Phe2181Ser
XM_011540044.1:c.6407T>C	XP_011538346.1:p.Phe2136Ser
XM_011540045.1:c.6542T>C	XP_011538347.1:p.Phe2181Ser
XM_011540046.1:c.6002T>C	XP_011538348.1:p.Phe2001Ser
XM_011540047.1:c.5360T>C	XP_011538349.1:p.Phe1787Ser
XM_011540048.1:c.6542T>C	XP_011538350.1:p.Phe2181Ser
XM_011540049.1:c.6542T>C	XP_011538351.1:p.Phe2181Ser
XM_011540050.1:c.6542T>C	XP_011538352.1:p.Phe2181Ser
XM_011540051.1:c.6542T>C	XP_011538353.1:p.Phe2181Ser
XM_011540052.1:c.2870T>C	XP_011538354.1:p.Phe957Ser
XR_945796.1:n.6785T>C
NM_022124.6:c.6347T>C MANE Select	NP_071407.4:p.Phe2116Ser